Canonical Allele Identifier: CA2351158779

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13316092T= , CM000682.2:g.13316092T= GRCh38
NC_000020.10:g.13296739T= , CM000682.1:g.13296739T= GRCh37
NC_000020.9:g.13244739T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937280.1:n.601-37A=
XM_017027680.1:c.878-8974T= (ISM1) XP_016883169.1:n.878-8974T=
XR_001754319.2:n.1282-37A= (TASP1)