Canonical Allele Identifier:
CA2008287868
Gene:
Linked Data
dbSNP Id:
rs1591429595
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.128870791C>T , CM000673.2:g.128870791C>T | GRCh38 |
| NC_000011.9:g.128740686C>T , CM000673.1:g.128740686C>T | GRCh37 |
| NC_000011.8:g.128245896C>T | NCBI36 |
| NG_009379.1:g.1583G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_948172.1:n.6120G>A | ||
| XR_948173.1:n.5809G>A |