Canonical Allele Identifier: CA453047359

Gene: SLC22A3

Linked Data

• gnomAD v4: 6-160436836-T-G
• MyVariant Identifiers: chr6:g.160857868T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160436836T>G , CM000668.2:g.160436836T>G	GRCh38
NC_000006.11:g.160857868T>G , CM000668.1:g.160857868T>G	GRCh37
NC_000006.10:g.160777858T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1032T>G MANE Select	ENSP00000275300.2:p.Thr344=
ENST00000275300.2:c.1032T>G	ENSP00000275300.2:p.Thr344=
NM_021977.3:c.1032T>G	NP_068812.1:p.Thr344=
XM_005267106.3:c.639T>G	XP_005267163.1:p.Thr213=
XM_011536075.1:c.576T>G	XP_011534377.1:p.Thr192=
XM_011536076.1:c.576T>G	XP_011534378.1:p.Thr192=
XM_011536077.1:c.576T>G	XP_011534379.1:p.Thr192=
XR_245546.1:n.1018-5925T>G
XM_005267106.5:c.639T>G	XP_005267163.1:p.Thr213=
XM_011536075.2:c.576T>G	XP_011534377.1:p.Thr192=
XM_011536076.3:c.576T>G	XP_011534378.1:p.Thr192=
XM_017011203.2:c.576T>G	XP_016866692.1:p.Thr192=
XR_001743588.1:n.1018-161T>G
XR_001743589.1:n.1018-5925T>G
NM_021977.4:c.1032T>G MANE Select	NP_068812.1:p.Thr344=