Canonical Allele Identifier: CA1015550534

Linked Data

dbSNP Id: rs560240136

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13316139A>G , CM000682.2:g.13316139A>G GRCh38
NC_000020.10:g.13296786A>G , CM000682.1:g.13296786A>G GRCh37
NC_000020.9:g.13244786A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937280.1:n.601-84T>C
XM_017027680.1:c.878-8927A>G (ISM1) XP_016883169.1:n.878-8927A>G
XR_001754319.2:n.1282-84T>C (TASP1)