Canonical Allele Identifier: CA2351158793

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13316133A= , CM000682.2:g.13316133A= GRCh38
NC_000020.10:g.13296780A= , CM000682.1:g.13296780A= GRCh37
NC_000020.9:g.13244780A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937280.1:n.601-78T=
XM_017027680.1:c.878-8933A= (ISM1) XP_016883169.1:n.878-8933A=
XR_001754319.2:n.1282-78T= (TASP1)