Canonical Allele Identifier: CA2724417739
Gene:

Linked Data

dbSNP Id: rs2134110558

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.81143477T>A , CM000673.2:g.81143477T>A GRCh38
NC_000011.9:g.80854520T>A , CM000673.1:g.80854520T>A GRCh37
NC_000011.8:g.80532168T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_247272.2:n.46+109449A>T