Linked Data
ClinVar Variation Id:
512342
dbSNP Id:
rs942245024
gnomAD v3:
6-152281975-C-T
gnomAD v4:
6-152281975-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152281975C>T , CM000668.2:g.152281975C>T | GRCh38 |
| NC_000006.11:g.152603110C>T , CM000668.1:g.152603110C>T | GRCh37 |
| NC_000006.10:g.152644803C>T | NCBI36 |
| NG_012855.1:g.360425G>A | |
| NG_012855.2:g.360425G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367255.10:c.18213G>A MANE Select | ENSP00000356224.5:p.Lys6071= | |
| ENST00000423061.6:c.18000G>A | ENSP00000396024.1:p.Lys6000= | |
| ENST00000341594.9:c.16998G>A | ENSP00000341887.6:p.Lys5666= | |
| ENST00000367255.9:c.18213G>A | ENSP00000356224.5:p.Lys6071= | |
| ENST00000367256.9:n.1905G>A | ||
| ENST00000409694.6:n.1797G>A | ||
| ENST00000423061.5:c.18000G>A | ENSP00000396024.1:p.Lys6000= | |
| ENST00000488376.2:n.68G>A | ||
| ENST00000489156.1:n.944G>A | ||
| NM_033071.3:c.18000G>A | NP_149062.1:p.Lys6000= | |
| NM_182961.3:c.18213G>A | NP_892006.3:p.Lys6071= | |
| XM_006715407.1:c.18246G>A | XP_006715470.1:p.Lys6082= | |
| XM_006715408.1:c.18234G>A | XP_006715471.1:p.Lys6078= | |
| XM_006715409.1:c.18225G>A | XP_006715472.1:p.Lys6075= | |
| XM_006715410.1:c.18246G>A | XP_006715473.1:p.Lys6082= | |
| XM_006715411.1:c.18195G>A | XP_006715474.1:p.Lys6065= | |
| XM_006715412.1:c.18234G>A | XP_006715475.1:p.Lys6078= | |
| XM_006715413.1:c.18246G>A | XP_006715476.1:p.Lys6082= | |
| XM_006715414.1:c.18174G>A | XP_006715477.1:p.Lys6058= | |
| XM_006715415.1:c.18246G>A | XP_006715478.1:p.Lys6082= | |
| XM_006715416.1:c.18234G>A | XP_006715479.1:p.Lys6078= | |
| XM_006715417.1:c.18105G>A | XP_006715480.1:p.Lys6035= | |
| XM_006715420.1:c.18093G>A | XP_006715483.1:p.Lys6031= | |
| XM_006715421.1:c.18090G>A | XP_006715484.1:p.Lys6030= | |
| XM_006715422.1:c.18087G>A | XP_006715485.1:p.Lys6029= | |
| XM_006715423.1:c.18246G>A | XP_006715486.1:p.Lys6082= | |
| XM_006715424.1:c.18246G>A | XP_006715487.1:p.Lys6082= | |
| XM_006715425.1:c.18246G>A | XP_006715488.1:p.Lys6082= | |
| XM_011535641.1:c.18246G>A | XP_011533943.1:p.Lys6082= | |
| XM_011535642.1:c.18234G>A | XP_011533944.1:p.Lys6078= | |
| XM_011535643.1:c.18081G>A | XP_011533945.1:p.Lys6027= | |
| XM_011535644.1:c.16521G>A | XP_011533946.1:p.Lys5507= | |
| XM_011535645.1:c.16014G>A | XP_011533947.1:p.Lys5338= | |
| XM_011535646.1:c.18246G>A | XP_011533948.1:p.Lys6082= | |
| XM_011535647.1:c.11481G>A | XP_011533949.1:p.Lys3827= | |
| XM_006715408.2:c.18234G>A | XP_006715471.1:p.Lys6078= | |
| XM_006715410.2:c.18246G>A | XP_006715473.1:p.Lys6082= | |
| XM_006715412.2:c.18234G>A | XP_006715475.1:p.Lys6078= | |
| XM_006715413.2:c.18246G>A | XP_006715476.1:p.Lys6082= | |
| XM_006715415.2:c.18246G>A | XP_006715478.1:p.Lys6082= | |
| XM_006715416.2:c.18234G>A | XP_006715479.1:p.Lys6078= | |
| XM_006715417.2:c.18105G>A | XP_006715480.1:p.Lys6035= | |
| XM_006715420.2:c.18093G>A | XP_006715483.1:p.Lys6031= | |
| XM_006715421.2:c.18090G>A | XP_006715484.1:p.Lys6030= | |
| XM_006715423.2:c.18246G>A | XP_006715486.1:p.Lys6082= | |
| XM_006715424.2:c.18246G>A | XP_006715487.1:p.Lys6082= | |
| XM_006715425.2:c.18246G>A | XP_006715488.1:p.Lys6082= | |
| XM_011535641.2:c.18246G>A | XP_011533943.1:p.Lys6082= | |
| XM_011535642.2:c.18234G>A | XP_011533944.1:p.Lys6078= | |
| XM_011535645.2:c.16014G>A | XP_011533947.1:p.Lys5338= | |
| XM_017010608.1:c.18246G>A | XP_016866097.1:p.Lys6082= | |
| XM_017010609.1:c.18246G>A | XP_016866098.1:p.Lys6082= | |
| XM_017010610.1:c.18225G>A | XP_016866099.1:p.Lys6075= | |
| XM_017010611.2:c.18219G>A | XP_016866100.1:p.Lys6073= | |
| XM_017010612.1:c.18168G>A | XP_016866101.1:p.Lys6056= | |
| XM_017010613.1:c.18246G>A | XP_016866102.1:p.Lys6082= | |
| XM_017010614.1:c.18093G>A | XP_016866103.1:p.Lys6031= | |
| XM_017010615.1:c.18093G>A | XP_016866104.1:p.Lys6031= | |
| XM_017010616.1:c.18246G>A | XP_016866105.1:p.Lys6082= | |
| XM_017010617.1:c.18246G>A | XP_016866106.1:p.Lys6082= | |
| XM_017010618.1:c.18234G>A | XP_016866107.1:p.Lys6078= | |
| XM_017010619.1:c.16521G>A | XP_016866108.1:p.Lys5507= | |
| XR_001743287.1:n.18729G>A | ||
| NM_182961.4:c.18213G>A MANE Select | NP_892006.3:p.Lys6071= | |
| NM_033071.5:c.18000G>A | NP_149062.2:p.Lys6000= |