Canonical Allele Identifier: CA16111318
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127132061G>A , CM000664.2:g.127132061G>A GRCh38
NC_000002.11:g.127889637G>A , CM000664.1:g.127889637G>A GRCh37
NC_000002.10:g.127606107G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923310.1:n.440-1177G>A
XR_923311.1:n.492-1177G>A
XR_923310.2:n.440-1177G>A
XR_923311.3:n.597-1177G>A