Canonical Allele Identifier: CA917652269
Gene: ADAMTS2 HGNC NCBI

Linked Data

dbSNP Id: rs1581150381
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.179143778_179143781del , CM000667.2:g.179143778_179143781del GRCh38
NC_000005.9:g.178570779_178570782del , CM000667.1:g.178570779_178570782del GRCh37
NC_000005.8:g.178503385_178503388del NCBI36
NG_023212.2:g.206553_206556del
NG_023212.3:g.206553_206556del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698889.1:c.1630-3741_1630-3738del ENSP00000514008.1:n.1630-3741_1630-3738del
ENST00000251582.12:c.1630-3741_1630-3738del MANE Select ENSP00000251582.7:n.1630-3741_1630-3738del
ENST00000518335.3:c.1630-3741_1630-3738del ENSP00000489888.2:n.1630-3741_1630-3738del
ENST00000251582.11:c.1630-3741_1630-3738del ENSP00000251582.7:n.1630-3741_1630-3738del
NM_014244.4:c.1630-3741_1630-3738del NP_055059.2:n.1630-3741_1630-3738del
NM_014244.5:c.1630-3741_1630-3738del MANE Select NP_055059.2:n.1630-3741_1630-3738del
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