Canonical Allele Identifier: CA366345792

Gene: SLC22A3

Linked Data

• MyVariant Identifiers: chr6:g.160858043T>G (hg19) ; chr6:g.160437011T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160437011T>G , CM000668.2:g.160437011T>G	GRCh38
NC_000006.11:g.160858043T>G , CM000668.1:g.160858043T>G	GRCh37
NC_000006.10:g.160778033T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1088T>G MANE Select	ENSP00000275300.2:p.Val363Gly
ENST00000275300.2:c.1088T>G	ENSP00000275300.2:p.Val363Gly
NM_021977.3:c.1088T>G	NP_068812.1:p.Val363Gly
XM_005267106.3:c.695T>G	XP_005267163.1:p.Val232Gly
XM_011536075.1:c.632T>G	XP_011534377.1:p.Val211Gly
XM_011536076.1:c.632T>G	XP_011534378.1:p.Val211Gly
XM_011536077.1:c.632T>G	XP_011534379.1:p.Val211Gly
XR_245546.1:n.1018-5750T>G
XM_005267106.5:c.695T>G	XP_005267163.1:p.Val232Gly
XM_011536075.2:c.632T>G	XP_011534377.1:p.Val211Gly
XM_011536076.3:c.632T>G	XP_011534378.1:p.Val211Gly
XM_017011203.2:c.632T>G	XP_016866692.1:p.Val211Gly
XR_001743588.1:n.1032T>G
XR_001743589.1:n.1018-5750T>G
NM_021977.4:c.1088T>G MANE Select	NP_068812.1:p.Val363Gly