Canonical Allele Identifier: CA821641259

Gene: SLC22A3

Linked Data

• dbSNP Id: rs1167263593
• gnomAD v3: 6-160387197-A-T
• gnomAD v4: 6-160387197-A-T
• MyVariant Identifiers: chr6:g.160808229A>T (hg19) ; chr6:g.160387197A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160387197A>T , CM000668.2:g.160387197A>T	GRCh38
NC_000006.11:g.160808229A>T , CM000668.1:g.160808229A>T	GRCh37
NC_000006.10:g.160728219A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.430-10782A>T MANE Select	ENSP00000275300.2:n.430-10782A>T
ENST00000275300.2:c.430-10782A>T	ENSP00000275300.2:n.430-10782A>T
NM_021977.3:c.430-10782A>T	NP_068812.1:n.430-10782A>T
XM_005267106.3:c.37-10782A>T	XP_005267163.1:n.37-10782A>T
XM_005267107.2:c.430-10782A>T	XP_005267164.1:n.430-10782A>T
XM_011536076.1:c.-27-10782A>T	XP_011534378.1:n.-27-10782A>T
XM_011536077.1:c.-27-10782A>T	XP_011534379.1:n.-27-10782A>T
XM_011536078.1:c.430-10782A>T	XP_011534380.1:n.430-10782A>T
XR_245546.1:n.472-10782A>T
XR_943187.1:n.4800T>A
XM_005267106.5:c.37-10782A>T	XP_005267163.1:n.37-10782A>T
XM_005267107.3:c.430-10782A>T	XP_005267164.1:n.430-10782A>T
XM_011536075.2:c.-5326A>T	XP_011534377.1:n.-5326A>T
XM_011536076.3:c.-27-10782A>T	XP_011534378.1:n.-27-10782A>T
XM_017011203.2:c.-27-10782A>T	XP_016866692.1:n.-27-10782A>T
XR_001743588.1:n.472-10782A>T
XR_001743589.1:n.472-10782A>T
NM_021977.4:c.430-10782A>T MANE Select	NP_068812.1:n.430-10782A>T