Canonical Allele Identifier: CA2351158795

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13316135T= , CM000682.2:g.13316135T= GRCh38
NC_000020.10:g.13296782T= , CM000682.1:g.13296782T= GRCh37
NC_000020.9:g.13244782T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937280.1:n.601-80A=
XM_017027680.1:c.878-8931T= (ISM1) XP_016883169.1:n.878-8931T=
XR_001754319.2:n.1282-80A= (TASP1)