Canonical Allele Identifier: CA2670948933
Gene: ADAMTS3 HGNC NCBI

Linked Data

gnomAD v4: 4-72313654-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313654A>T , CM000666.2:g.72313654A>T GRCh38
NC_000004.11:g.73179371A>T , CM000666.1:g.73179371A>T GRCh37
NC_000004.10:g.73398235A>T NCBI36
NG_046955.1:g.260146T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000286657.10:c.1745+23T>A MANE Select ENSP00000286657.4:n.1745+23T>A
ENST00000286657.8:c.1745+23T>A ENSP00000286657.4:n.1745+23T>A
ENST00000622135.1:c.1745+23T>A ENSP00000480055.1:n.1745+23T>A
NM_014243.2:c.1745+23T>A NP_055058.2:n.1745+23T>A
XM_011532421.1:c.1688+23T>A XP_011530723.1:n.1688+23T>A
XM_011532422.1:c.1661+23T>A XP_011530724.1:n.1661+23T>A
XM_011532423.1:c.1103+23T>A XP_011530725.1:n.1103+23T>A
XM_011532424.1:c.1013+23T>A XP_011530726.1:n.1013+23T>A
XM_011532421.2:c.1688+23T>A XP_011530723.1:n.1688+23T>A
XM_011532422.3:c.1661+23T>A XP_011530724.1:n.1661+23T>A
NM_014243.3:c.1745+23T>A MANE Select NP_055058.2:n.1745+23T>A
Search 100 bp 5'
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