Canonical Allele Identifier: CA12465536
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.45968511G>A , CM000669.2:g.45968511G>A GRCh38
NC_000007.13:g.46008110G>A , CM000669.1:g.46008110G>A GRCh37
NC_000007.12:g.45974635G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927237.1:n.322-9008G>A
XR_927238.1:n.322-9008G>A
XR_927239.1:n.322-9008G>A
XR_927240.1:n.322-9008G>A
XR_001745202.1:n.327-9008G>A
XR_001745203.1:n.327-9008G>A