Canonical Allele Identifier: CA1467600159
Gene: ADAMTS3 HGNC NCBI

Linked Data

dbSNP Id: rs1719318879

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313994G>T , CM000666.2:g.72313994G>T GRCh38
NC_000004.11:g.73179711G>T , CM000666.1:g.73179711G>T GRCh37
NC_000004.10:g.73398575G>T NCBI36
NG_046955.1:g.259806C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1600-172C>A MANE Select ENSP00000286657.4:n.1600-172C>A
ENST00000286657.8:c.1600-172C>A ENSP00000286657.4:n.1600-172C>A
ENST00000622135.1:c.1600-172C>A ENSP00000480055.1:n.1600-172C>A
NM_014243.2:c.1600-172C>A NP_055058.2:n.1600-172C>A
XM_011532421.1:c.1543-172C>A XP_011530723.1:n.1543-172C>A
XM_011532422.1:c.1516-172C>A XP_011530724.1:n.1516-172C>A
XM_011532423.1:c.958-172C>A XP_011530725.1:n.958-172C>A
XM_011532424.1:c.868-172C>A XP_011530726.1:n.868-172C>A
XM_011532421.2:c.1543-172C>A XP_011530723.1:n.1543-172C>A
XM_011532422.3:c.1516-172C>A XP_011530724.1:n.1516-172C>A
NM_014243.3:c.1600-172C>A MANE Select NP_055058.2:n.1600-172C>A