Canonical Allele Identifier: CA1267947391
Gene:

Linked Data

dbSNP Id: rs1672676800

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016206G>A , CM000664.2:g.88016206G>A GRCh38
NC_000002.11:g.88315725G>A , CM000664.1:g.88315725G>A GRCh37
NC_000002.10:g.88096840G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.551G>A
XR_940336.3:n.551G>A