Canonical Allele Identifier: CA1870932939
Gene:

Linked Data

dbSNP Id: rs1826972682

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108092813C>T , CM000671.2:g.108092813C>T GRCh38
NC_000009.11:g.110855094C>T , CM000671.1:g.110855094C>T GRCh37
NC_000009.10:g.109894915C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930239.1:n.461-39519G>A
XR_001746881.1:n.668-39519G>A
XR_001746882.1:n.668-39519G>A