Canonical Allele Identifier: CA1563552055
Gene:

Linked Data

dbSNP Id: rs1744563384

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222732A>G , CM000667.2:g.92222732A>G GRCh38
NC_000005.9:g.91518549A>G , CM000667.1:g.91518549A>G GRCh37
NC_000005.8:g.91554305A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948565.1:n.394+18048A>G