Canonical Allele Identifier: CA1467600073
Gene: ADAMTS3 HGNC NCBI

Linked Data

dbSNP Id: rs1719315205
gnomAD v4: 4-72313886-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313886C>T , CM000666.2:g.72313886C>T GRCh38
NC_000004.11:g.73179603C>T , CM000666.1:g.73179603C>T GRCh37
NC_000004.10:g.73398467C>T NCBI36
NG_046955.1:g.259914G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1600-64G>A MANE Select ENSP00000286657.4:n.1600-64G>A
ENST00000286657.8:c.1600-64G>A ENSP00000286657.4:n.1600-64G>A
ENST00000622135.1:c.1600-64G>A ENSP00000480055.1:n.1600-64G>A
NM_014243.2:c.1600-64G>A NP_055058.2:n.1600-64G>A
XM_011532421.1:c.1543-64G>A XP_011530723.1:n.1543-64G>A
XM_011532422.1:c.1516-64G>A XP_011530724.1:n.1516-64G>A
XM_011532423.1:c.958-64G>A XP_011530725.1:n.958-64G>A
XM_011532424.1:c.868-64G>A XP_011530726.1:n.868-64G>A
XM_011532421.2:c.1543-64G>A XP_011530723.1:n.1543-64G>A
XM_011532422.3:c.1516-64G>A XP_011530724.1:n.1516-64G>A
NM_014243.3:c.1600-64G>A MANE Select NP_055058.2:n.1600-64G>A