Canonical Allele Identifier: CA2740558701
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499934G>T , CM000666.2:g.102499934G>T GRCh38
NC_000004.11:g.103421091G>T , CM000666.1:g.103421091G>T GRCh37
NC_000004.10:g.103640123G>T NCBI36
NG_050628.1:g.3606G>T

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1315C>A XP_011530769.1:n.643+1315C>A
NR_136202.1:n.48+2505C>A