Canonical Allele Identifier: CA1563552066
Gene:

Linked Data

dbSNP Id: rs1744563830

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222751G>A , CM000667.2:g.92222751G>A GRCh38
NC_000005.9:g.91518568G>A , CM000667.1:g.91518568G>A GRCh37
NC_000005.8:g.91554324G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948565.1:n.394+18067G>A