Canonical Allele Identifier:
CA1870932950
Gene:
Linked Data
dbSNP Id:
rs1826972849
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.108092824G>T , CM000671.2:g.108092824G>T | GRCh38 |
| NC_000009.11:g.110855105G>T , CM000671.1:g.110855105G>T | GRCh37 |
| NC_000009.10:g.109894926G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930239.1:n.461-39530C>A | ||
| XR_001746881.1:n.668-39530C>A | ||
| XR_001746882.1:n.668-39530C>A |