Canonical Allele Identifier: CA496590133

Gene: ADAMTS18

Linked Data

• gnomAD v4: 16-77335788-G-C
• MyVariant Identifiers: chr16:g.77369685G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77335788G>C , CM000678.2:g.77335788G>C	GRCh38
NC_000016.9:g.77369685G>C , CM000678.1:g.77369685G>C	GRCh37
NC_000016.8:g.75927186G>C	NCBI36
NG_031879.1:g.104327C>G
NG_031879.2:g.104327C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282849.10:c.1827C>G MANE Select	ENSP00000282849.5:p.Val609=
ENST00000282849.9:c.1827C>G	ENSP00000282849.5:p.Val609=
NM_199355.2:c.1827C>G	NP_955387.1:p.Val609=
XM_006721158.2:c.-89C>G	XP_006721221.1:n.-89C>G
XM_011522923.1:c.1311C>G	XP_011521225.1:p.Val437=
XM_011522924.1:c.1311C>G	XP_011521226.1:p.Val437=
NM_001326358.1:c.1311C>G	NP_001313287.1:p.Val437=
NM_199355.3:c.1827C>G	NP_955387.1:p.Val609=
XM_011522924.2:c.1311C>G	XP_011521226.1:p.Val437=
XM_017022988.2:c.591C>G	XP_016878477.1:p.Val197=
XM_017022989.1:c.591C>G	XP_016878478.1:p.Val197=
NM_199355.4:c.1827C>G MANE Select	NP_955387.1:p.Val609=
NM_001326358.2:c.1311C>G	NP_001313287.1:p.Val437=