Canonical Allele Identifier: CA1038979700
Gene:

Linked Data

dbSNP Id: rs577409855

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168260588T>A , CM000664.2:g.168260588T>A GRCh38
NC_000002.11:g.169117098T>A , CM000664.1:g.169117098T>A GRCh37
NC_000002.10:g.168825344T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739763.1:n.912-4508T>A
XR_001739764.1:n.318-4508T>A
XR_001739765.1:n.436-4508T>A