Canonical Allele Identifier: CA2351158842

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13316275T= , CM000682.2:g.13316275T= GRCh38
NC_000020.10:g.13296922T= , CM000682.1:g.13296922T= GRCh37
NC_000020.9:g.13244922T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937280.1:n.601-220A=
XM_017027680.1:c.878-8791T= (ISM1) XP_016883169.1:n.878-8791T=
XR_001754319.2:n.1282-220A= (TASP1)