Linked Data
dbSNP Id:
rs772773024
ExAC:
12:132425833 C / T
gnomAD v2:
12-132425833-C-T
gnomAD v4:
12-131941288-C-T
MyVariant Identifiers:
chr12:g.132425833C>T (hg19)
chr12:g.132425833_132425834delinsTT (hg19)
chr12:g.131941288C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.131941288C>T , CM000674.2:g.131941288C>T | GRCh38 |
| NC_000012.11:g.132425833C>T , CM000674.1:g.132425833C>T | GRCh37 |
| NC_000012.10:g.130991786C>T | NCBI36 |
| NG_013039.1:g.17089C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376649.8:c.545-4C>T MANE Select | ENSP00000365837.3:n.545-4C>T | |
| ENST00000322060.9:c.461-4C>T | ENSP00000324726.5:n.461-4C>T | |
| ENST00000376649.7:c.545-4C>T | ENSP00000365837.3:n.545-4C>T | |
| ENST00000443358.6:c.461-4C>T | ENSP00000392451.2:n.461-4C>T | |
| ENST00000535067.5:c.358-2251C>T | ENSP00000443969.1:n.358-2251C>T | |
| ENST00000537484.1:c.470-4C>T | ENSP00000440179.1:n.470-4C>T | |
| ENST00000542167.2:c.386-4C>T | ENSP00000438948.1:n.386-4C>T | |
| ENST00000543754.1:n.362C>T | ||
| NM_001002019.2:c.461-4C>T | NP_001002019.1:n.461-4C>T | |
| NM_001002020.2:c.461-4C>T | NP_001002020.1:n.461-4C>T | |
| NM_025215.5:c.545-4C>T | NP_079491.2:n.545-4C>T | |
| XM_011538768.1:c.146-4C>T | XP_011537070.1:n.146-4C>T | |
| XM_011538768.3:c.146-4C>T | XP_011537070.1:n.146-4C>T | |
| XR_001748872.1:n.1000-4C>T | ||
| NM_001002019.3:c.461-4C>T | NP_001002019.1:n.461-4C>T | |
| NM_001002020.3:c.461-4C>T | NP_001002020.1:n.461-4C>T | |
| NM_025215.6:c.545-4C>T MANE Select | NP_079491.2:n.545-4C>T |