Canonical Allele Identifier: CA2234465134
Gene: ADAMTS18 HGNC NCBI

Linked Data

dbSNP Id: rs1567537190

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.77393769G>T , CM000678.2:g.77393769G>T GRCh38
NC_000016.9:g.77427666G>T , CM000678.1:g.77427666G>T GRCh37
NC_000016.8:g.75985167G>T NCBI36
NG_031879.1:g.46346C>A
NG_031879.2:g.46346C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282849.10:c.496-26046C>A MANE Select ENSP00000282849.5:n.496-26046C>A
ENST00000282849.9:c.496-26046C>A ENSP00000282849.5:n.496-26046C>A
ENST00000449265.2:c.496-26046C>A ENSP00000392540.2:n.496-26046C>A
ENST00000562345.1:c.294-26100C>A
ENST00000564369.1:n.422-26046C>A
ENST00000567121.5:n.353-26046C>A
ENST00000567914.1:n.340-26046C>A
ENST00000569309.1:n.453-14790C>A
NM_199355.2:c.496-26046C>A NP_955387.1:n.496-26046C>A
XM_011522923.1:c.-25-26046C>A XP_011521225.1:n.-25-26046C>A
XM_011522924.1:c.-25-26046C>A XP_011521226.1:n.-25-26046C>A
NM_001326358.1:c.-25-26046C>A NP_001313287.1:n.-25-26046C>A
NM_199355.3:c.496-26046C>A NP_955387.1:n.496-26046C>A
XM_011522924.2:c.-25-26046C>A XP_011521226.1:n.-25-26046C>A
XM_017022988.2:c.-585-26046C>A XP_016878477.1:n.-585-26046C>A
XM_017022989.1:c.-581-26046C>A XP_016878478.1:n.-581-26046C>A
NM_199355.4:c.496-26046C>A MANE Select NP_955387.1:n.496-26046C>A
NM_001326358.2:c.-25-26046C>A NP_001313287.1:n.-25-26046C>A