Canonical Allele Identifier: CA1350284006
Gene:

Linked Data

dbSNP Id: rs1698203543

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.21207112A>G , CM000665.2:g.21207112A>G GRCh38
NC_000003.11:g.21248604A>G , CM000665.1:g.21248604A>G GRCh37
NC_000003.10:g.21223608A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940646.1:n.254-3886A>G
XR_940646.2:n.547-3886A>G