Linked Data
dbSNP Id:
rs2058215933
gnomAD v3:
6-152140100-C-T
gnomAD v4:
6-152140100-C-T
MyVariant Identifiers:
chr6:g.152461235C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152140100C>T , CM000668.2:g.152140100C>T | GRCh38 |
| NC_000006.11:g.152461235C>T , CM000668.1:g.152461235C>T | GRCh37 |
| NC_000006.10:g.152502928C>T | NCBI36 |
| NG_012855.1:g.502300G>A | |
| NG_012855.2:g.502300G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354674.5:c.1842G>A MANE Plus Clinical | ENSP00000346701.4:p.Lys614= | |
| ENST00000367255.10:c.25308G>A MANE Select | ENSP00000356224.5:p.Lys8436= | |
| ENST00000423061.6:c.25164G>A | ENSP00000396024.1:p.Lys8388= | |
| ENST00000672154.1:c.710G>A | ||
| ENST00000672169.1:c.1043G>A | ||
| ENST00000673173.1:c.952G>A | ||
| ENST00000673451.1:c.1080G>A | ENSP00000500189.1:p.Lys360= | |
| ENST00000341594.9:c.24093G>A | ENSP00000341887.6:p.Lys8031= | |
| ENST00000347037.9:n.2056G>A | ||
| ENST00000354674.4:c.1842G>A | ENSP00000346701.4:p.Lys614= | |
| ENST00000367251.7:c.4143G>A | ENSP00000356220.3:p.Lys1381= | |
| ENST00000367255.9:c.25308G>A | ENSP00000356224.5:p.Lys8436= | |
| ENST00000367256.9:n.9000G>A | ||
| ENST00000367257.8:c.3246G>A | ENSP00000356226.4:p.Lys1082= | |
| ENST00000409694.6:n.8892G>A | ||
| ENST00000423061.5:c.25164G>A | ENSP00000396024.1:p.Lys8388= | |
| ENST00000460912.6:n.1922G>A | ||
| ENST00000478916.5:n.4330G>A | ||
| ENST00000536990.5:n.2145G>A | ||
| ENST00000539504.5:c.1773G>A | ENSP00000441052.1:p.Lys591= | |
| NM_033071.3:c.25164G>A | NP_149062.1:p.Lys8388= | |
| NM_182961.3:c.25308G>A | NP_892006.3:p.Lys8436= | |
| XM_006715407.1:c.25413G>A | XP_006715470.1:p.Lys8471= | |
| XM_006715408.1:c.25401G>A | XP_006715471.1:p.Lys8467= | |
| XM_006715409.1:c.25392G>A | XP_006715472.1:p.Lys8464= | |
| XM_006715410.1:c.25413G>A | XP_006715473.1:p.Lys8471= | |
| XM_006715411.1:c.25362G>A | XP_006715474.1:p.Lys8454= | |
| XM_006715412.1:c.25398G>A | XP_006715475.1:p.Lys8466= | |
| XM_006715413.1:c.25344G>A | XP_006715476.1:p.Lys8448= | |
| XM_006715414.1:c.25341G>A | XP_006715477.1:p.Lys8447= | |
| XM_006715415.1:c.25344G>A | XP_006715478.1:p.Lys8448= | |
| XM_006715416.1:c.25329G>A | XP_006715479.1:p.Lys8443= | |
| XM_006715417.1:c.25272G>A | XP_006715480.1:p.Lys8424= | |
| XM_006715420.1:c.25260G>A | XP_006715483.1:p.Lys8420= | |
| XM_006715421.1:c.25257G>A | XP_006715484.1:p.Lys8419= | |
| XM_006715422.1:c.25254G>A | XP_006715485.1:p.Lys8418= | |
| XM_006715423.1:c.25413G>A | XP_006715486.1:p.Lys8471= | |
| XM_006715424.1:c.25413G>A | XP_006715487.1:p.Lys8471= | |
| XM_006715425.1:c.25344G>A | XP_006715488.1:p.Lys8448= | |
| XM_011535641.1:c.25410G>A | XP_011533943.1:p.Lys8470= | |
| XM_011535642.1:c.25398G>A | XP_011533944.1:p.Lys8466= | |
| XM_011535643.1:c.25248G>A | XP_011533945.1:p.Lys8416= | |
| XM_011535644.1:c.23688G>A | XP_011533946.1:p.Lys7896= | |
| XM_011535645.1:c.23181G>A | XP_011533947.1:p.Lys7727= | |
| XM_011535647.1:c.18648G>A | XP_011533949.1:p.Lys6216= | |
| NM_001347701.1:c.1914G>A | NP_001334630.1:p.Lys638= | |
| NM_001347702.1:c.1842G>A | NP_001334631.1:p.Lys614= | |
| XM_006715408.2:c.25401G>A | XP_006715471.1:p.Lys8467= | |
| XM_006715410.2:c.25413G>A | XP_006715473.1:p.Lys8471= | |
| XM_006715412.2:c.25398G>A | XP_006715475.1:p.Lys8466= | |
| XM_006715413.2:c.25344G>A | XP_006715476.1:p.Lys8448= | |
| XM_006715415.2:c.25344G>A | XP_006715478.1:p.Lys8448= | |
| XM_006715416.2:c.25329G>A | XP_006715479.1:p.Lys8443= | |
| XM_006715417.2:c.25272G>A | XP_006715480.1:p.Lys8424= | |
| XM_006715420.2:c.25260G>A | XP_006715483.1:p.Lys8420= | |
| XM_006715421.2:c.25257G>A | XP_006715484.1:p.Lys8419= | |
| XM_006715423.2:c.25413G>A | XP_006715486.1:p.Lys8471= | |
| XM_006715424.2:c.25413G>A | XP_006715487.1:p.Lys8471= | |
| XM_006715425.2:c.25344G>A | XP_006715488.1:p.Lys8448= | |
| XM_011535641.2:c.25410G>A | XP_011533943.1:p.Lys8470= | |
| XM_011535642.2:c.25398G>A | XP_011533944.1:p.Lys8466= | |
| XM_011535645.2:c.23181G>A | XP_011533947.1:p.Lys7727= | |
| XM_017010608.1:c.25413G>A | XP_016866097.1:p.Lys8471= | |
| XM_017010609.1:c.25413G>A | XP_016866098.1:p.Lys8471= | |
| XM_017010610.1:c.25392G>A | XP_016866099.1:p.Lys8464= | |
| XM_017010611.2:c.25386G>A | XP_016866100.1:p.Lys8462= | |
| XM_017010612.1:c.25335G>A | XP_016866101.1:p.Lys8445= | |
| XM_017010613.1:c.25341G>A | XP_016866102.1:p.Lys8447= | |
| XM_017010614.1:c.25257G>A | XP_016866103.1:p.Lys8419= | |
| XM_017010615.1:c.25188G>A | XP_016866104.1:p.Lys8396= | |
| XM_017010616.1:c.25344G>A | XP_016866105.1:p.Lys8448= | |
| XM_017010617.1:c.25341G>A | XP_016866106.1:p.Lys8447= | |
| XM_017010618.1:c.25329G>A | XP_016866107.1:p.Lys8443= | |
| XM_017010619.1:c.23688G>A | XP_016866108.1:p.Lys7896= | |
| NM_182961.4:c.25308G>A MANE Select | NP_892006.3:p.Lys8436= | |
| NM_001347701.2:c.1914G>A | NP_001334630.1:p.Lys638= | |
| NM_001347702.2:c.1842G>A MANE Plus Clinical | NP_001334631.1:p.Lys614= | |
| NM_033071.5:c.25164G>A | NP_149062.2:p.Lys8388= |