Canonical Allele Identifier: CA1481405886
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499967G= , CM000666.2:g.102499967G= GRCh38
NC_000004.11:g.103421124G= , CM000666.1:g.103421124G= GRCh37
NC_000004.10:g.103640156G= NCBI36
NG_050628.1:g.3639G=

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1282C= XP_011530769.1:n.643+1282C=
NR_136202.1:n.48+2472C=