Canonical Allele Identifier: CA585052428
Gene:

Linked Data

dbSNP Id: rs1266150400

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999529A>G , CM000670.2:g.126999529A>G GRCh38
NC_000008.10:g.128011774A>G , CM000670.1:g.128011774A>G GRCh37
NC_000008.9:g.128080956A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-7026A>G