Linked Data
ClinVar Variation Id:
1035198
ClinVar RCV Id:
RCV001338033
dbSNP Id:
rs876658288
gnomAD v4:
16-23641120-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23641120T>A , CM000678.2:g.23641120T>A | GRCh38 |
| NC_000016.9:g.23652441T>A , CM000678.1:g.23652441T>A | GRCh37 |
| NC_000016.8:g.23559942T>A | NCBI36 |
| NG_007406.1:g.5238A>T , LRG_308:g.5238A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561514.3:c.-815A>T | ENSP00000460666.3:n.-815A>T | |
| ENST00000565038.2:c.38A>T | ENSP00000459882.2:p.Glu13Val | |
| ENST00000566069.6:c.38A>T | ENSP00000459237.2:p.Glu13Val | |
| ENST00000697377.2:c.-202A>T | ENSP00000513286.2:n.-202A>T | |
| ENST00000697379.2:c.-108A>T | ENSP00000513287.2:n.-108A>T | |
| ENST00000561514.2:c.-1706A>T | ENSP00000460666.2:n.-1706A>T | |
| ENST00000697374.1:c.-1297A>T | ENSP00000513284.1:n.-1297A>T | |
| ENST00000697376.1:c.-1018A>T | ENSP00000513285.1:n.-1018A>T | |
| ENST00000697377.1:c.-1093A>T | ENSP00000513286.1:n.-1093A>T | |
| ENST00000697379.1:c.-999A>T | ENSP00000513287.1:n.-999A>T | |
| ENST00000697382.1:c.-1757A>T | ENSP00000513288.1:n.-1757A>T | |
| ENST00000697383.1:c.38A>T | ENSP00000513289.1:p.Glu13Val | |
| ENST00000697384.1:n.192A>T | ||
| ENST00000261584.9:c.38A>T MANE Select | ENSP00000261584.4:p.Glu13Val | |
| ENST00000261584.8:c.38A>T | ENSP00000261584.4:p.Glu13Val | |
| ENST00000567003.1:n.182A>T | ||
| ENST00000568219.5:c.-838+7A>T | ENSP00000454703.2:n.-838+7A>T | |
| NM_024675.3:c.38A>T , LRG_308t1:c.38A>T | NP_078951.2:p.Glu13Val | |
| XM_011545948.1:c.-982A>T | XP_011544250.1:n.-982A>T | |
| XM_011545946.2:c.-815A>T | XP_011544248.1:n.-815A>T | |
| XM_011545947.2:c.-815A>T | XP_011544249.1:n.-815A>T | |
| XM_011545948.2:c.-982A>T | XP_011544250.1:n.-982A>T | |
| XM_017023671.1:c.-815A>T | XP_016879160.1:n.-815A>T | |
| XM_017023672.2:c.38A>T | XP_016879161.1:p.Glu13Val | |
| XM_017023673.2:c.38A>T | XP_016879162.1:p.Glu13Val | |
| NM_024675.4:c.38A>T MANE Select | NP_078951.2:p.Glu13Val |