Canonical Allele Identifier: CA185688670
Gene:

Linked Data

dbSNP Id: rs1017926418

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999533T>G , CM000670.2:g.126999533T>G GRCh38
NC_000008.10:g.128011778T>G , CM000670.1:g.128011778T>G GRCh37
NC_000008.9:g.128080960T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-7022T>G