Canonical Allele Identifier: CA9745071

Gene: ADAM33

Linked Data

• dbSNP Id: rs749593008
• ExAC: 20:3650266 G / A
• gnomAD v2: 20-3650266-G-A
• gnomAD v3: 20-3669619-G-A
• gnomAD v4: 20-3669619-G-A
• MyVariant Identifiers: chr20:g.3650266G>A (hg19) ; chr20:g.3669619G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669619G>A , CM000682.2:g.3669619G>A	GRCh38
NC_000020.10:g.3650266G>A , CM000682.1:g.3650266G>A	GRCh37
NC_000020.9:g.3598266G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2259C>T MANE Select	ENSP00000348912.3:p.His753=
ENST00000350009.6:c.2181C>T	ENSP00000322550.5:p.His727=
ENST00000356518.6:c.2259C>T	ENSP00000348912.2:p.His753=
ENST00000379861.8:c.2259C>T	ENSP00000369190.4:p.His753=
ENST00000466620.5:n.1820C>T
ENST00000483362.1:n.1007C>T
ENST00000617732.1:c.*946C>T	ENSP00000483343.1:n.*946C>T
ENST00000619289.4:c.1899C>T	ENSP00000484600.1:p.His633=
NM_001282447.1:c.2259C>T	NP_001269376.1:p.His753=
NM_025220.3:c.2259C>T	NP_079496.1:p.His753=
NM_153202.2:c.2181C>T	NP_694882.1:p.His727=
XM_005260843.1:c.2298C>T	XP_005260900.1:p.His766=
XM_006723639.1:c.2298C>T	XP_006723702.1:p.His766=
XM_006723640.1:c.2289C>T	XP_006723703.1:p.His763=
XM_011529366.1:c.2295C>T	XP_011527668.1:p.His765=
XM_011529367.1:c.2256C>T	XP_011527669.1:p.His752=
XM_011529368.1:c.2220C>T	XP_011527670.1:p.His740=
XM_011529373.1:c.1296C>T	XP_011527675.1:p.His432=
XR_937151.1:n.2384-249C>T
XR_937152.1:n.2384-249C>T
XR_937153.1:n.2283C>T
XR_937154.1:n.2283C>T
XR_937155.1:n.2204C>T
XR_937157.1:n.2206C>T
NM_001282447.2:c.2259C>T	NP_001269376.1:p.His753=
NM_025220.4:c.2259C>T	NP_079496.1:p.His753=
NM_153202.3:c.2181C>T	NP_694882.1:p.His727=
XM_011529373.2:c.1296C>T	XP_011527675.1:p.His432=
XR_001754405.1:n.2370C>T
XR_002958534.1:n.2479C>T
NM_001282447.3:c.2259C>T	NP_001269376.1:p.His753=
NM_025220.5:c.2259C>T MANE Select	NP_079496.1:p.His753=
NM_153202.4:c.2181C>T	NP_694882.1:p.His727=