Canonical Allele Identifier: CA2351158776

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13316083T= , CM000682.2:g.13316083T= GRCh38
NC_000020.10:g.13296730T= , CM000682.1:g.13296730T= GRCh37
NC_000020.9:g.13244730T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937280.1:n.601-28A=
XM_017027680.1:c.878-8983T= (ISM1) XP_016883169.1:n.878-8983T=
XR_001754319.2:n.1282-28A= (TASP1)