Canonical Allele Identifier: CA1149396971
Gene:

Linked Data

dbSNP Id: rs1659182744

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036486G>A , CM000663.2:g.2036486G>A GRCh38
NC_000001.10:g.1967925G>A , CM000663.1:g.1967925G>A GRCh37
NC_000001.9:g.1957785G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946823.1:n.722C>T
XR_001737845.2:n.725C>T
XR_946823.3:n.725C>T