Canonical Allele Identifier: CA1986002871
Gene:

Linked Data

dbSNP Id: rs1565159227

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.81143364A>G , CM000673.2:g.81143364A>G GRCh38
NC_000011.9:g.80854407A>G , CM000673.1:g.80854407A>G GRCh37
NC_000011.8:g.80532055A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247272.2:n.46+109562T>C