Canonical Allele Identifier: CA1563552132
Gene:

Linked Data

dbSNP Id: rs1744565716

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222891G>A , CM000667.2:g.92222891G>A GRCh38
NC_000005.9:g.91518708G>A , CM000667.1:g.91518708G>A GRCh37
NC_000005.8:g.91554464G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948565.1:n.394+18207G>A