Canonical Allele Identifier: CA2351158796

Linked Data

dbSNP Id: rs2040601909

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13316135T>C , CM000682.2:g.13316135T>C GRCh38
NC_000020.10:g.13296782T>C , CM000682.1:g.13296782T>C GRCh37
NC_000020.9:g.13244782T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937280.1:n.601-80A>G
XM_017027680.1:c.878-8931T>C (ISM1) XP_016883169.1:n.878-8931T>C
XR_001754319.2:n.1282-80A>G (TASP1)