Canonical Allele Identifier: CA16265952
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.57982677G>A , CM000668.2:g.57982677G>A GRCh38
NC_000006.11:g.58308955G>A , CM000668.1:g.58308955G>A GRCh37
NC_000006.10:g.58416914G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926906.1:n.321+11021G>A
XR_001744180.1:n.3471+11021G>A
XR_001744183.1:n.3471+11021G>A
XR_001744184.1:n.3471+11021G>A
XR_001744185.1:n.3471+11021G>A