Linked Data
dbSNP Id:
rs1259132501
gnomAD v2:
1-186143580-C-T
gnomAD v3:
1-186174448-C-T
gnomAD v4:
1-186174448-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186174448C>T , CM000663.2:g.186174448C>T | GRCh38 |
| NC_000001.10:g.186143580C>T , CM000663.1:g.186143580C>T | GRCh37 |
| NC_000001.9:g.184410203C>T | NCBI36 |
| NG_011841.1:g.444898C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271588.9:c.15815-66C>T MANE Select | ENSP00000271588.4:n.15815-66C>T | |
| ENST00000271588.8:c.15815-66C>T | ENSP00000271588.4:n.15815-66C>T | |
| ENST00000414277.1:c.191-66C>T | ENSP00000406205.1:n.191-66C>T | |
| NM_031935.2:c.15815-66C>T | NP_114141.2:n.15815-66C>T | |
| XM_011510037.1:c.15530-66C>T | XP_011508339.1:n.15530-66C>T | |
| XM_011510038.1:c.15815-66C>T | XP_011508340.1:n.15815-66C>T | |
| XM_011510038.3:c.15815-66C>T | XP_011508340.1:n.15815-66C>T | |
| XM_017002437.1:c.13838-66C>T | XP_016857926.1:n.13838-66C>T | |
| NM_031935.3:c.15815-66C>T MANE Select | NP_114141.2:n.15815-66C>T |