Canonical Allele Identifier: CA2351158787

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13316119C= , CM000682.2:g.13316119C= GRCh38
NC_000020.10:g.13296766C= , CM000682.1:g.13296766C= GRCh37
NC_000020.9:g.13244766C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937280.1:n.601-64G=
XM_017027680.1:c.878-8947C= (ISM1) XP_016883169.1:n.878-8947C=
XR_001754319.2:n.1282-64G= (TASP1)