Canonical Allele Identifier: CA1481407039
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501002A= , CM000666.2:g.102501002A= GRCh38
NC_000004.11:g.103422159A= , CM000666.1:g.103422159A= GRCh37
NC_000004.10:g.103641191A= NCBI36
NG_050628.1:g.4674A=

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+247T= XP_011530769.1:n.643+247T=
NR_136202.1:n.48+1437T=