Linked Data
ClinVar Variation Id:
502587
dbSNP Id:
rs759556319
ExAC:
6:152583209 C / A
gnomAD v2:
6-152583209-C-A
gnomAD v3:
6-152262074-C-A
gnomAD v4:
6-152262074-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152262074C>A , CM000668.2:g.152262074C>A | GRCh38 |
| NC_000006.11:g.152583209C>A , CM000668.1:g.152583209C>A | GRCh37 |
| NC_000006.10:g.152624902C>A | NCBI36 |
| NG_012855.1:g.380326G>T | |
| NG_012855.2:g.380326G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367255.10:c.18930G>T MANE Select | ENSP00000356224.5:p.Gln6310His | |
| ENST00000423061.6:c.18717G>T | ENSP00000396024.1:p.Gln6239His | |
| ENST00000341594.9:c.17715G>T | ENSP00000341887.6:p.Gln5905His | |
| ENST00000367255.9:c.18930G>T | ENSP00000356224.5:p.Gln6310His | |
| ENST00000367256.9:n.2622G>T | ||
| ENST00000409694.6:n.2514G>T | ||
| ENST00000423061.5:c.18717G>T | ENSP00000396024.1:p.Gln6239His | |
| ENST00000545694.1:n.231G>T | ||
| NM_033071.3:c.18717G>T | NP_149062.1:p.Gln6239His | |
| NM_182961.3:c.18930G>T | NP_892006.3:p.Gln6310His | |
| XM_006715407.1:c.18966G>T | XP_006715470.1:p.Gln6322His | |
| XM_006715408.1:c.18954G>T | XP_006715471.1:p.Gln6318His | |
| XM_006715409.1:c.18945G>T | XP_006715472.1:p.Gln6315His | |
| XM_006715410.1:c.18966G>T | XP_006715473.1:p.Gln6322His | |
| XM_006715411.1:c.18915G>T | XP_006715474.1:p.Gln6305His | |
| XM_006715412.1:c.18951G>T | XP_006715475.1:p.Gln6317His | |
| XM_006715413.1:c.18966G>T | XP_006715476.1:p.Gln6322His | |
| XM_006715414.1:c.18894G>T | XP_006715477.1:p.Gln6298His | |
| XM_006715415.1:c.18966G>T | XP_006715478.1:p.Gln6322His | |
| XM_006715416.1:c.18951G>T | XP_006715479.1:p.Gln6317His | |
| XM_006715417.1:c.18825G>T | XP_006715480.1:p.Gln6275His | |
| XM_006715420.1:c.18813G>T | XP_006715483.1:p.Gln6271His | |
| XM_006715421.1:c.18810G>T | XP_006715484.1:p.Gln6270His | |
| XM_006715422.1:c.18807G>T | XP_006715485.1:p.Gln6269His | |
| XM_006715423.1:c.18966G>T | XP_006715486.1:p.Gln6322His | |
| XM_006715424.1:c.18966G>T | XP_006715487.1:p.Gln6322His | |
| XM_006715425.1:c.18966G>T | XP_006715488.1:p.Gln6322His | |
| XM_011535641.1:c.18963G>T | XP_011533943.1:p.Gln6321His | |
| XM_011535642.1:c.18951G>T | XP_011533944.1:p.Gln6317His | |
| XM_011535643.1:c.18801G>T | XP_011533945.1:p.Gln6267His | |
| XM_011535644.1:c.17241G>T | XP_011533946.1:p.Gln5747His | |
| XM_011535645.1:c.16734G>T | XP_011533947.1:p.Gln5578His | |
| XM_011535646.1:c.18966G>T | XP_011533948.1:p.Gln6322His | |
| XM_011535647.1:c.12201G>T | XP_011533949.1:p.Gln4067His | |
| XM_006715408.2:c.18954G>T | XP_006715471.1:p.Gln6318His | |
| XM_006715410.2:c.18966G>T | XP_006715473.1:p.Gln6322His | |
| XM_006715412.2:c.18951G>T | XP_006715475.1:p.Gln6317His | |
| XM_006715413.2:c.18966G>T | XP_006715476.1:p.Gln6322His | |
| XM_006715415.2:c.18966G>T | XP_006715478.1:p.Gln6322His | |
| XM_006715416.2:c.18951G>T | XP_006715479.1:p.Gln6317His | |
| XM_006715417.2:c.18825G>T | XP_006715480.1:p.Gln6275His | |
| XM_006715420.2:c.18813G>T | XP_006715483.1:p.Gln6271His | |
| XM_006715421.2:c.18810G>T | XP_006715484.1:p.Gln6270His | |
| XM_006715423.2:c.18966G>T | XP_006715486.1:p.Gln6322His | |
| XM_006715424.2:c.18966G>T | XP_006715487.1:p.Gln6322His | |
| XM_006715425.2:c.18966G>T | XP_006715488.1:p.Gln6322His | |
| XM_011535641.2:c.18963G>T | XP_011533943.1:p.Gln6321His | |
| XM_011535642.2:c.18951G>T | XP_011533944.1:p.Gln6317His | |
| XM_011535645.2:c.16734G>T | XP_011533947.1:p.Gln5578His | |
| XM_017010608.1:c.18966G>T | XP_016866097.1:p.Gln6322His | |
| XM_017010609.1:c.18966G>T | XP_016866098.1:p.Gln6322His | |
| XM_017010610.1:c.18945G>T | XP_016866099.1:p.Gln6315His | |
| XM_017010611.2:c.18939G>T | XP_016866100.1:p.Gln6313His | |
| XM_017010612.1:c.18888G>T | XP_016866101.1:p.Gln6296His | |
| XM_017010613.1:c.18963G>T | XP_016866102.1:p.Gln6321His | |
| XM_017010614.1:c.18810G>T | XP_016866103.1:p.Gln6270His | |
| XM_017010615.1:c.18810G>T | XP_016866104.1:p.Gln6270His | |
| XM_017010616.1:c.18966G>T | XP_016866105.1:p.Gln6322His | |
| XM_017010617.1:c.18963G>T | XP_016866106.1:p.Gln6321His | |
| XM_017010618.1:c.18951G>T | XP_016866107.1:p.Gln6317His | |
| XM_017010619.1:c.17241G>T | XP_016866108.1:p.Gln5747His | |
| XR_001743287.1:n.19449G>T | ||
| NM_182961.4:c.18930G>T MANE Select | NP_892006.3:p.Gln6310His | |
| NM_033071.5:c.18717G>T | NP_149062.2:p.Gln6239His |