Canonical Allele Identifier: CA623592047

Gene: ADAMTS18

Linked Data

• dbSNP Id: rs1450515222
• gnomAD v2: 16-77427582-C-A
• gnomAD v3: 16-77393685-C-A
• gnomAD v4: 16-77393685-C-A
• MyVariant Identifiers: chr16:g.77427582C>A (hg19) ; chr16:g.77393685C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77393685C>A , CM000678.2:g.77393685C>A	GRCh38
NC_000016.9:g.77427582C>A , CM000678.1:g.77427582C>A	GRCh37
NC_000016.8:g.75985083C>A	NCBI36
NG_031879.1:g.46430G>T
NG_031879.2:g.46430G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282849.10:c.496-25962G>T MANE Select	ENSP00000282849.5:n.496-25962G>T
ENST00000282849.9:c.496-25962G>T	ENSP00000282849.5:n.496-25962G>T
ENST00000449265.2:c.496-25962G>T	ENSP00000392540.2:n.496-25962G>T
ENST00000562345.1:c.294-26016G>T
ENST00000564369.1:n.422-25962G>T
ENST00000567121.5:n.353-25962G>T
ENST00000567914.1:n.340-25962G>T
ENST00000569309.1:n.453-14706G>T
NM_199355.2:c.496-25962G>T	NP_955387.1:n.496-25962G>T
XM_011522923.1:c.-25-25962G>T	XP_011521225.1:n.-25-25962G>T
XM_011522924.1:c.-25-25962G>T	XP_011521226.1:n.-25-25962G>T
NM_001326358.1:c.-25-25962G>T	NP_001313287.1:n.-25-25962G>T
NM_199355.3:c.496-25962G>T	NP_955387.1:n.496-25962G>T
XM_011522924.2:c.-25-25962G>T	XP_011521226.1:n.-25-25962G>T
XM_017022988.2:c.-585-25962G>T	XP_016878477.1:n.-585-25962G>T
XM_017022989.1:c.-581-25962G>T	XP_016878478.1:n.-581-25962G>T
NM_199355.4:c.496-25962G>T MANE Select	NP_955387.1:n.496-25962G>T
NM_001326358.2:c.-25-25962G>T	NP_001313287.1:n.-25-25962G>T