Canonical Allele Identifier: CA1015550564

Linked Data

dbSNP Id: rs2040602529

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13316223del , CM000682.2:g.13316223del GRCh38
NC_000020.10:g.13296870del , CM000682.1:g.13296870del GRCh37
NC_000020.9:g.13244870del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937280.1:n.601-167del
XM_017027680.1:c.878-8843del (ISM1) XP_016883169.1:n.878-8843del
XR_001754319.2:n.1282-167del (TASP1)