Canonical Allele Identifier: CA2351158789

Linked Data

dbSNP Id: rs2040601694

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13316123T>C , CM000682.2:g.13316123T>C GRCh38
NC_000020.10:g.13296770T>C , CM000682.1:g.13296770T>C GRCh37
NC_000020.9:g.13244770T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937280.1:n.601-68A>G
XM_017027680.1:c.878-8943T>C (ISM1) XP_016883169.1:n.878-8943T>C
XR_001754319.2:n.1282-68A>G (TASP1)