Canonical Allele Identifier: CA1481405902
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499984A= , CM000666.2:g.102499984A= GRCh38
NC_000004.11:g.103421141A= , CM000666.1:g.103421141A= GRCh37
NC_000004.10:g.103640173A= NCBI36
NG_050628.1:g.3656A=

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1265T= XP_011530769.1:n.643+1265T=
NR_136202.1:n.48+2455T=