Canonical Allele Identifier: CA1207463727
Gene:

Linked Data

dbSNP Id: rs1660425056

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172741773C>A , CM000663.2:g.172741773C>A GRCh38
NC_000001.10:g.172710913C>A , CM000663.1:g.172710913C>A GRCh37
NC_000001.9:g.170977536C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922289.1:n.27-34046C>A