Canonical Allele Identifier: CA1870932947
Gene:

Linked Data

dbSNP Id: rs1826972825

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108092823T>A , CM000671.2:g.108092823T>A GRCh38
NC_000009.11:g.110855104T>A , CM000671.1:g.110855104T>A GRCh37
NC_000009.10:g.109894925T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930239.1:n.461-39529A>T
XR_001746881.1:n.668-39529A>T
XR_001746882.1:n.668-39529A>T