Canonical Allele Identifier: CA2234464978
Gene: ADAMTS18 HGNC NCBI

Linked Data

dbSNP Id: rs1597217859

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.77393556A>G , CM000678.2:g.77393556A>G GRCh38
NC_000016.9:g.77427453A>G , CM000678.1:g.77427453A>G GRCh37
NC_000016.8:g.75984954A>G NCBI36
NG_031879.1:g.46559T>C
NG_031879.2:g.46559T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282849.10:c.496-25833T>C MANE Select ENSP00000282849.5:n.496-25833T>C
ENST00000282849.9:c.496-25833T>C ENSP00000282849.5:n.496-25833T>C
ENST00000449265.2:c.496-25833T>C ENSP00000392540.2:n.496-25833T>C
ENST00000562345.1:c.294-25887T>C
ENST00000564369.1:n.422-25833T>C
ENST00000567121.5:n.353-25833T>C
ENST00000567914.1:n.340-25833T>C
ENST00000569309.1:n.453-14577T>C
NM_199355.2:c.496-25833T>C NP_955387.1:n.496-25833T>C
XM_011522923.1:c.-25-25833T>C XP_011521225.1:n.-25-25833T>C
XM_011522924.1:c.-25-25833T>C XP_011521226.1:n.-25-25833T>C
NM_001326358.1:c.-25-25833T>C NP_001313287.1:n.-25-25833T>C
NM_199355.3:c.496-25833T>C NP_955387.1:n.496-25833T>C
XM_011522924.2:c.-25-25833T>C XP_011521226.1:n.-25-25833T>C
XM_017022988.2:c.-585-25833T>C XP_016878477.1:n.-585-25833T>C
XM_017022989.1:c.-581-25833T>C XP_016878478.1:n.-581-25833T>C
NM_199355.4:c.496-25833T>C MANE Select NP_955387.1:n.496-25833T>C
NM_001326358.2:c.-25-25833T>C NP_001313287.1:n.-25-25833T>C