Canonical Allele Identifier: CA1207463738
Gene:

Linked Data

dbSNP Id: rs1660425335

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172741799T>A , CM000663.2:g.172741799T>A GRCh38
NC_000001.10:g.172710939T>A , CM000663.1:g.172710939T>A GRCh37
NC_000001.9:g.170977562T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922289.1:n.27-34020T>A