Canonical Allele Identifier: CA1149397013
Gene:

Linked Data

dbSNP Id: rs1659183673

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036544C>A , CM000663.2:g.2036544C>A GRCh38
NC_000001.10:g.1967983C>A , CM000663.1:g.1967983C>A GRCh37
NC_000001.9:g.1957843C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946823.1:n.664G>T
XR_001737845.2:n.667G>T
XR_946823.3:n.667G>T