Canonical Allele Identifier: CA59054661
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155400189G>A , CM000664.2:g.155400189G>A GRCh38
NC_000002.11:g.156256701G>A , CM000664.1:g.156256701G>A GRCh37
NC_000002.10:g.155964947G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923496.1:n.47-4077G>A
XR_923496.2:n.223-4077G>A