Canonical Allele Identifier: CA2234465132

Gene: ADAMTS18

Linked Data

• dbSNP Id: rs1567537190

Genomic Alleles

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

Transcript Alleles

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