Canonical Allele Identifier: CA1563552192
Gene:

Linked Data

dbSNP Id: rs1580346926

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222998T>A , CM000667.2:g.92222998T>A GRCh38
NC_000005.9:g.91518815T>A , CM000667.1:g.91518815T>A GRCh37
NC_000005.8:g.91554571T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948565.1:n.394+18314T>A