Linked Data
dbSNP Id:
rs1776012772
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32390271C>T , CM000668.2:g.32390271C>T | GRCh38 |
| NC_000006.11:g.32358048C>T , CM000668.1:g.32358048C>T | GRCh37 |
| NC_000006.10:g.32466026C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011515039.1:c.482-15183C>T | XP_011513341.1:n.482-15183C>T | |
| NR_136245.1:n.303-15183C>T |