Canonical Allele Identifier: CA741343005

Linked Data

dbSNP Id: rs1446943580

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13316271del , CM000682.2:g.13316271del GRCh38
NC_000020.10:g.13296918del , CM000682.1:g.13296918del GRCh37
NC_000020.9:g.13244918del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937280.1:n.601-216del
XM_017027680.1:c.878-8795del (ISM1) XP_016883169.1:n.878-8795del
XR_001754319.2:n.1282-216del (TASP1)