Canonical Allele Identifier: CA2676856133
Gene: ADAMTS2 HGNC NCBI

Linked Data

gnomAD v4: 5-179129835-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.179129835A>T , CM000667.2:g.179129835A>T GRCh38
NC_000005.9:g.178556836A>T , CM000667.1:g.178556836A>T GRCh37
NC_000005.8:g.178489442A>T NCBI36
NG_023212.2:g.220494T>A
NG_023212.3:g.220494T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000698889.1:c.2457+97T>A ENSP00000514008.1:n.2457+97T>A
ENST00000251582.12:c.2457+97T>A MANE Select ENSP00000251582.7:n.2457+97T>A
ENST00000518335.3:c.2457+97T>A ENSP00000489888.2:n.2457+97T>A
ENST00000251582.11:c.2457+97T>A ENSP00000251582.7:n.2457+97T>A
NM_014244.4:c.2457+97T>A NP_055059.2:n.2457+97T>A
NM_014244.5:c.2457+97T>A MANE Select NP_055059.2:n.2457+97T>A
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