Canonical Allele Identifier: CA2502475118
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499972C>T , CM000666.2:g.102499972C>T GRCh38
NC_000004.11:g.103421129C>T , CM000666.1:g.103421129C>T GRCh37
NC_000004.10:g.103640161C>T NCBI36
NG_050628.1:g.3644C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1277G>A XP_011530769.1:n.643+1277G>A
NR_136202.1:n.48+2467G>A