Canonical Allele Identifier: CA453047687

Gene: SLC22A3

Linked Data

• gnomAD v4: 6-160437195-T-C
• MyVariant Identifiers: chr6:g.160858227T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160437195T>C , CM000668.2:g.160437195T>C	GRCh38
NC_000006.11:g.160858227T>C , CM000668.1:g.160858227T>C	GRCh37
NC_000006.10:g.160778217T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1272T>C MANE Select	ENSP00000275300.2:p.Thr424=
ENST00000275300.2:c.1272T>C	ENSP00000275300.2:p.Thr424=
NM_021977.3:c.1272T>C	NP_068812.1:p.Thr424=
XM_005267106.3:c.879T>C	XP_005267163.1:p.Thr293=
XM_011536075.1:c.816T>C	XP_011534377.1:p.Thr272=
XM_011536076.1:c.816T>C	XP_011534378.1:p.Thr272=
XM_011536077.1:c.816T>C	XP_011534379.1:p.Thr272=
XR_245546.1:n.1018-5566T>C
XM_005267106.5:c.879T>C	XP_005267163.1:p.Thr293=
XM_011536075.2:c.816T>C	XP_011534377.1:p.Thr272=
XM_011536076.3:c.816T>C	XP_011534378.1:p.Thr272=
XM_017011203.2:c.816T>C	XP_016866692.1:p.Thr272=
XR_001743588.1:n.1216T>C
XR_001743589.1:n.1018-5566T>C
NM_021977.4:c.1272T>C MANE Select	NP_068812.1:p.Thr424=