Canonical Allele Identifier: CA2351158782

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13316101A= , CM000682.2:g.13316101A= GRCh38
NC_000020.10:g.13296748A= , CM000682.1:g.13296748A= GRCh37
NC_000020.9:g.13244748A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937280.1:n.601-46T=
XM_017027680.1:c.878-8965A= (ISM1) XP_016883169.1:n.878-8965A=
XR_001754319.2:n.1282-46T= (TASP1)