Canonical Allele Identifier: CA2762880459
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499896C>A , CM000666.2:g.102499896C>A GRCh38
NC_000004.11:g.103421053C>A , CM000666.1:g.103421053C>A GRCh37
NC_000004.10:g.103640085C>A NCBI36
NG_050628.1:g.3568C>A

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1353G>T XP_011530769.1:n.643+1353G>T
NR_136202.1:n.48+2543G>T