Canonical Allele Identifier: CA724136004

Gene: ADAMTS18

Linked Data

• dbSNP Id: rs1157531436
• gnomAD v3: 16-77396619-G-A
• gnomAD v4: 16-77396619-G-A
• MyVariant Identifiers: chr16:g.77430516G>A (hg19) ; chr16:g.77396619G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77396619G>A , CM000678.2:g.77396619G>A	GRCh38
NC_000016.9:g.77430516G>A , CM000678.1:g.77430516G>A	GRCh37
NC_000016.8:g.75988017G>A	NCBI36
NG_031879.1:g.43496C>T
NG_031879.2:g.43496C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000282849.10:c.496-28896C>T MANE Select	ENSP00000282849.5:n.496-28896C>T
ENST00000282849.9:c.496-28896C>T	ENSP00000282849.5:n.496-28896C>T
ENST00000449265.2:c.496-28896C>T	ENSP00000392540.2:n.496-28896C>T
ENST00000562345.1:c.294-28950C>T
ENST00000564369.1:n.422-28896C>T
ENST00000567121.5:n.353-28896C>T
ENST00000567914.1:n.340-28896C>T
ENST00000569309.1:n.453-17640C>T
NM_199355.2:c.496-28896C>T	NP_955387.1:n.496-28896C>T
XM_011522923.1:c.-25-28896C>T	XP_011521225.1:n.-25-28896C>T
XM_011522924.1:c.-25-28896C>T	XP_011521226.1:n.-25-28896C>T
NM_001326358.1:c.-25-28896C>T	NP_001313287.1:n.-25-28896C>T
NM_199355.3:c.496-28896C>T	NP_955387.1:n.496-28896C>T
XM_011522924.2:c.-25-28896C>T	XP_011521226.1:n.-25-28896C>T
XM_017022988.2:c.-585-28896C>T	XP_016878477.1:n.-585-28896C>T
XM_017022989.1:c.-581-28896C>T	XP_016878478.1:n.-581-28896C>T
NM_199355.4:c.496-28896C>T MANE Select	NP_955387.1:n.496-28896C>T
NM_001326358.2:c.-25-28896C>T	NP_001313287.1:n.-25-28896C>T