Canonical Allele Identifier: CA185688673
Gene:

Linked Data

dbSNP Id: rs1009377466

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999558A>G , CM000670.2:g.126999558A>G GRCh38
NC_000008.10:g.128011803A>G , CM000670.1:g.128011803A>G GRCh37
NC_000008.9:g.128080985A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-6997A>G