Canonical Allele Identifier: CA2522599407

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13316116C>G , CM000682.2:g.13316116C>G GRCh38
NC_000020.10:g.13296763C>G , CM000682.1:g.13296763C>G GRCh37
NC_000020.9:g.13244763C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937280.1:n.601-61G>C
XM_017027680.1:c.878-8950C>G (ISM1) XP_016883169.1:n.878-8950C>G
XR_001754319.2:n.1282-61G>C (TASP1)