Canonical Allele Identifier: CA35069269
Gene:

Linked Data

dbSNP Id: rs182788550

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800676C>A , CM000663.2:g.192800676C>A GRCh38
NC_000001.10:g.192769806C>A , CM000663.1:g.192769806C>A GRCh37
NC_000001.9:g.191036429C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429211.2:n.106C>A