Canonical Allele Identifier: CA1207463744
Gene:

Linked Data

dbSNP Id: rs1660425494

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172741808A>C , CM000663.2:g.172741808A>C GRCh38
NC_000001.10:g.172710948A>C , CM000663.1:g.172710948A>C GRCh37
NC_000001.9:g.170977571A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922289.1:n.27-34011A>C