Canonical Allele Identifier: CA81296277
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs1164064

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743553G>A , CM000665.2:g.109743553G>A GRCh38
NC_000003.11:g.109462400G>A , CM000665.1:g.109462400G>A GRCh37
NC_000003.10:g.110945090G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924325.1:n.142+63358G>A