Canonical Allele Identifier: CA55082032
Gene:

Linked Data

dbSNP Id: rs564995561

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122883952G>A , CM000664.2:g.122883952G>A GRCh38
NC_000002.11:g.123641528G>A , CM000664.1:g.123641528G>A GRCh37
NC_000002.10:g.123357998G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923292.1:n.1125-990G>A
XR_001739692.1:n.1451-990G>A
XR_923292.2:n.1358-990G>A