Canonical Allele Identifier:
CA1870933050
Gene:
Linked Data
dbSNP Id:
rs1826976165
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.108093064G>T , CM000671.2:g.108093064G>T | GRCh38 |
| NC_000009.11:g.110855345G>T , CM000671.1:g.110855345G>T | GRCh37 |
| NC_000009.10:g.109895166G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930239.1:n.461-39770C>A | ||
| XR_001746881.1:n.668-39770C>A | ||
| XR_001746882.1:n.668-39770C>A |