Canonical Allele Identifier: CA1870933031
Gene:

Linked Data

dbSNP Id: rs1826975779

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108093000T>A , CM000671.2:g.108093000T>A GRCh38
NC_000009.11:g.110855281T>A , CM000671.1:g.110855281T>A GRCh37
NC_000009.10:g.109895102T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930239.1:n.461-39706A>T
XR_001746881.1:n.668-39706A>T
XR_001746882.1:n.668-39706A>T