Canonical Allele Identifier: CA1481405942
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500011A= , CM000666.2:g.102500011A= GRCh38
NC_000004.11:g.103421168A= , CM000666.1:g.103421168A= GRCh37
NC_000004.10:g.103640200A= NCBI36
NG_050628.1:g.3683A=

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1238T= XP_011530769.1:n.643+1238T=
NR_136202.1:n.48+2428T=