Linked Data
dbSNP Id:
rs1170382207
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.177442541A>T , CM000666.2:g.177442541A>T | GRCh38 |
| NC_000004.11:g.178363695A>T , CM000666.1:g.178363695A>T | GRCh37 |
| NC_000004.10:g.178600689A>T | NCBI36 |
| NG_011845.2:g.4963T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001741929.1:n.42A>T |