Linked Data
ClinVar Variation Id:
95682
ClinVar RCV Id:
RCV000081715
RCV000292444
RCV000331197
RCV001573175
RCV001093742
RCV002294019
RCV002498430
dbSNP Id:
rs139767853
ExAC:
1:5927943 G / A
gnomAD v2:
1-5927943-G-A
gnomAD v3:
1-5867883-G-A
gnomAD v4:
1-5867883-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.5867883G>A , CM000663.2:g.5867883G>A | GRCh38 |
| NC_000001.10:g.5927943G>A , CM000663.1:g.5927943G>A | GRCh37 |
| NC_000001.9:g.5850530G>A | NCBI36 |
| NG_011724.2:g.129589C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378156.9:c.3329C>T MANE Select | ENSP00000367398.4:p.Ala1110Val | |
| ENST00000378156.8:c.3329C>T | ENSP00000367398.4:p.Ala1110Val | |
| ENST00000378161.5:n.493C>T | ||
| ENST00000378169.7:c.*2230C>T | ENSP00000367411.3:n.*2230C>T | |
| ENST00000468253.1:n.604C>T | ||
| ENST00000478423.6:n.3061C>T | ||
| ENST00000489180.6:c.*1140C>T | ENSP00000423747.1:n.*1140C>T | |
| NM_001291593.1:c.1790C>T | NP_001278522.1:p.Ala597Val | |
| NM_001291594.1:c.1793C>T | NP_001278523.1:p.Ala598Val | |
| NM_015102.4:c.3329C>T | NP_055917.1:p.Ala1110Val | |
| NR_111987.1:n.4144C>T | ||
| XM_006710563.2:c.3329C>T | XP_006710626.1:p.Ala1110Val | |
| XM_006710565.2:c.3329C>T | XP_006710628.1:p.Ala1110Val | |
| XM_011541213.1:c.3326C>T | XP_011539515.1:p.Ala1109Val | |
| XM_011541214.1:c.3287C>T | XP_011539516.1:p.Ala1096Val | |
| XM_011541215.1:c.3218C>T | XP_011539517.1:p.Ala1073Val | |
| XM_011541216.1:c.3329C>T | XP_011539518.1:p.Ala1110Val | |
| XM_011541217.1:c.3329C>T | XP_011539519.1:p.Ala1110Val | |
| XM_011541218.1:c.3329C>T | XP_011539520.1:p.Ala1110Val | |
| XM_011541219.1:c.3275C>T | XP_011539521.1:p.Ala1092Val | |
| XM_011541220.1:c.3329C>T | XP_011539522.1:p.Ala1110Val | |
| XR_946604.1:n.3180C>T | ||
| XM_006710563.3:c.3329C>T | XP_006710626.1:p.Ala1110Val | |
| XM_011541216.2:c.3329C>T | XP_011539518.1:p.Ala1110Val | |
| XM_011541217.2:c.3329C>T | XP_011539519.1:p.Ala1110Val | |
| XM_011541218.2:c.3329C>T | XP_011539520.1:p.Ala1110Val | |
| XM_017000996.1:c.3284C>T | XP_016856485.1:p.Ala1095Val | |
| XM_017000997.1:c.3329C>T | XP_016856486.1:p.Ala1110Val | |
| XM_017000998.1:c.3329C>T | XP_016856487.1:p.Ala1110Val | |
| XM_017000999.1:c.2801C>T | XP_016856488.1:p.Ala934Val | |
| XM_017001000.2:c.2801C>T | XP_016856489.1:p.Ala934Val | |
| XM_017001001.1:c.2531C>T | XP_016856490.1:p.Ala844Val | |
| XM_017001003.1:c.1790C>T | XP_016856492.1:p.Ala597Val | |
| XR_001737114.1:n.3367C>T | ||
| XR_001737115.1:n.3180C>T | ||
| NM_015102.5:c.3329C>T MANE Select | NP_055917.1:p.Ala1110Val | |
| NM_001291593.2:c.1790C>T | NP_001278522.1:p.Ala597Val | |
| NM_001291594.2:c.1793C>T | NP_001278523.1:p.Ala598Val | |
| NR_111987.2:n.4096C>T |