Linked Data
ClinVar Variation Id:
556961
ClinVar RCV Id:
RCV000673035
RCV000778223
RCV000806323
RCV001252803
RCV002249400
RCV002271560
RCV002531329
dbSNP Id:
rs199669988
ExAC:
1:21890590 G / A
gnomAD v2:
1-21890590-G-A
gnomAD v3:
1-21564097-G-A
gnomAD v4:
1-21564097-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.21564097G>A , CM000663.2:g.21564097G>A | GRCh38 |
| NC_000001.10:g.21890590G>A , CM000663.1:g.21890590G>A | GRCh37 |
| NC_000001.9:g.21763177G>A | NCBI36 |
| NG_008940.1:g.59733G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000374840.8:c.529G>A MANE Select | ENSP00000363973.3:p.Ala177Thr | |
| ENST00000374832.5:c.529G>A | ENSP00000363965.1:p.Ala177Thr | |
| ENST00000374840.7:c.529G>A | ENSP00000363973.3:p.Ala177Thr | |
| ENST00000468526.1:n.589G>A | ||
| ENST00000539907.5:c.298G>A | ENSP00000437674.1:p.Ala100Thr | |
| ENST00000540617.5:c.364G>A | ENSP00000442672.1:p.Ala122Thr | |
| NM_000478.4:c.529G>A | NP_000469.3:p.Ala177Thr | |
| NM_001127501.2:c.364G>A | NP_001120973.2:p.Ala122Thr | |
| NM_001177520.1:c.298G>A | NP_001170991.1:p.Ala100Thr | |
| XM_005245818.1:c.529G>A | XP_005245875.1:p.Ala177Thr | |
| XM_005245820.2:c.529G>A | XP_005245877.1:p.Ala177Thr | |
| XM_006710546.1:c.529G>A | XP_006710609.1:p.Ala177Thr | |
| NM_000478.5:c.529G>A | NP_000469.3:p.Ala177Thr | |
| NM_001127501.3:c.364G>A | NP_001120973.2:p.Ala122Thr | |
| NM_001177520.2:c.298G>A | NP_001170991.1:p.Ala100Thr | |
| XM_006710546.3:c.529G>A | XP_006710609.1:p.Ala177Thr | |
| XM_017000903.1:c.373G>A | XP_016856392.1:p.Ala125Thr | |
| NM_000478.6:c.529G>A MANE Select | NP_000469.3:p.Ala177Thr | |
| NM_001127501.4:c.364G>A | NP_001120973.2:p.Ala122Thr | |
| NM_001177520.3:c.298G>A | NP_001170991.1:p.Ala100Thr | |
| NM_001369803.2:c.529G>A | NP_001356732.1:p.Ala177Thr | |
| NM_001369804.2:c.529G>A | NP_001356733.1:p.Ala177Thr | |
| NM_001369805.2:c.529G>A | NP_001356734.1:p.Ala177Thr |