Canonical Allele Identifier: CA453047369

Gene: SLC22A3

Linked Data

• dbSNP Id: rs760511764
• gnomAD v3: 6-160436857-A-T
• gnomAD v4: 6-160436857-A-T
• MyVariant Identifiers: chr6:g.160857889A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160436857A>T , CM000668.2:g.160436857A>T	GRCh38
NC_000006.11:g.160857889A>T , CM000668.1:g.160857889A>T	GRCh37
NC_000006.10:g.160777879A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1053A>T MANE Select	ENSP00000275300.2:p.Thr351=
ENST00000275300.2:c.1053A>T	ENSP00000275300.2:p.Thr351=
NM_021977.3:c.1053A>T	NP_068812.1:p.Thr351=
XM_005267106.3:c.660A>T	XP_005267163.1:p.Thr220=
XM_011536075.1:c.597A>T	XP_011534377.1:p.Thr199=
XM_011536076.1:c.597A>T	XP_011534378.1:p.Thr199=
XM_011536077.1:c.597A>T	XP_011534379.1:p.Thr199=
XR_245546.1:n.1018-5904A>T
XM_005267106.5:c.660A>T	XP_005267163.1:p.Thr220=
XM_011536075.2:c.597A>T	XP_011534377.1:p.Thr199=
XM_011536076.3:c.597A>T	XP_011534378.1:p.Thr199=
XM_017011203.2:c.597A>T	XP_016866692.1:p.Thr199=
XR_001743588.1:n.1018-140A>T
XR_001743589.1:n.1018-5904A>T
NM_021977.4:c.1053A>T MANE Select	NP_068812.1:p.Thr351=