Canonical Allele Identifier: CA2351158822

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13316220A= , CM000682.2:g.13316220A= GRCh38
NC_000020.10:g.13296867A= , CM000682.1:g.13296867A= GRCh37
NC_000020.9:g.13244867A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937280.1:n.601-165T=
XM_017027680.1:c.878-8846A= (ISM1) XP_016883169.1:n.878-8846A=
XR_001754319.2:n.1282-165T= (TASP1)