Canonical Allele Identifier: CA1481405824
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499885T= , CM000666.2:g.102499885T= GRCh38
NC_000004.11:g.103421042T= , CM000666.1:g.103421042T= GRCh37
NC_000004.10:g.103640074T= NCBI36
NG_050628.1:g.3557T=

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1364A= XP_011530769.1:n.643+1364A=
NR_136202.1:n.48+2554A=