Canonical Allele Identifier: CA2676855531
Gene: ADAMTS2 HGNC NCBI

Linked Data

gnomAD v4: 5-179127935-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.179127939del , CM000667.2:g.179127939del GRCh38
NC_000005.9:g.178554940del , CM000667.1:g.178554940del GRCh37
NC_000005.8:g.178487546del NCBI36
NG_023212.2:g.222393del
NG_023212.3:g.222393del

Transcript Alleles

HGVS Amino-acid change
ENST00000698889.1:c.2617+23del ENSP00000514008.1:n.2617+23del
ENST00000251582.12:c.2617+23del MANE Select ENSP00000251582.7:n.2617+23del
ENST00000518335.3:c.2617+23del ENSP00000489888.2:n.2617+23del
ENST00000251582.11:c.2617+23del ENSP00000251582.7:n.2617+23del
NM_014244.4:c.2617+23del NP_055059.2:n.2617+23del
NM_014244.5:c.2617+23del MANE Select NP_055059.2:n.2617+23del
Search 100 bp 5'
Search 100 bp 3'