Canonical Allele Identifier: CA453047353

Gene: SLC22A3

Linked Data

• MyVariant Identifiers: chr6:g.160857862G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160436830G>C , CM000668.2:g.160436830G>C	GRCh38
NC_000006.11:g.160857862G>C , CM000668.1:g.160857862G>C	GRCh37
NC_000006.10:g.160777852G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1026G>C MANE Select	ENSP00000275300.2:p.Val342=
ENST00000275300.2:c.1026G>C	ENSP00000275300.2:p.Val342=
NM_021977.3:c.1026G>C	NP_068812.1:p.Val342=
XM_005267106.3:c.633G>C	XP_005267163.1:p.Val211=
XM_011536075.1:c.570G>C	XP_011534377.1:p.Val190=
XM_011536076.1:c.570G>C	XP_011534378.1:p.Val190=
XM_011536077.1:c.570G>C	XP_011534379.1:p.Val190=
XR_245546.1:n.1018-5931G>C
XM_005267106.5:c.633G>C	XP_005267163.1:p.Val211=
XM_011536075.2:c.570G>C	XP_011534377.1:p.Val190=
XM_011536076.3:c.570G>C	XP_011534378.1:p.Val190=
XM_017011203.2:c.570G>C	XP_016866692.1:p.Val190=
XR_001743588.1:n.1018-167G>C
XR_001743589.1:n.1018-5931G>C
NM_021977.4:c.1026G>C MANE Select	NP_068812.1:p.Val342=