Canonical Allele Identifier: CA1563552179
Gene:

Linked Data

dbSNP Id: rs1580346918

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222981G>C , CM000667.2:g.92222981G>C GRCh38
NC_000005.9:g.91518798G>C , CM000667.1:g.91518798G>C GRCh37
NC_000005.8:g.91554554G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948565.1:n.394+18297G>C