Canonical Allele Identifier: CA1677048002

Gene: SLC22A3

Linked Data

• dbSNP Id: rs1583466318

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160387054G>C , CM000668.2:g.160387054G>C	GRCh38
NC_000006.11:g.160808086G>C , CM000668.1:g.160808086G>C	GRCh37
NC_000006.10:g.160728076G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000275300.3:c.430-10925G>C MANE Select	ENSP00000275300.2:n.430-10925G>C
ENST00000275300.2:c.430-10925G>C	ENSP00000275300.2:n.430-10925G>C
NM_021977.3:c.430-10925G>C	NP_068812.1:n.430-10925G>C
XM_005267106.3:c.37-10925G>C	XP_005267163.1:n.37-10925G>C
XM_005267107.2:c.430-10925G>C	XP_005267164.1:n.430-10925G>C
XM_011536076.1:c.-27-10925G>C	XP_011534378.1:n.-27-10925G>C
XM_011536077.1:c.-27-10925G>C	XP_011534379.1:n.-27-10925G>C
XM_011536078.1:c.430-10925G>C	XP_011534380.1:n.430-10925G>C
XR_245546.1:n.472-10925G>C
XR_943187.1:n.4943C>G
XM_005267106.5:c.37-10925G>C	XP_005267163.1:n.37-10925G>C
XM_005267107.3:c.430-10925G>C	XP_005267164.1:n.430-10925G>C
XM_011536075.2:c.-5469G>C	XP_011534377.1:n.-5469G>C
XM_011536076.3:c.-27-10925G>C	XP_011534378.1:n.-27-10925G>C
XM_017011203.2:c.-27-10925G>C	XP_016866692.1:n.-27-10925G>C
XR_001743588.1:n.472-10925G>C
XR_001743589.1:n.472-10925G>C
NM_021977.4:c.430-10925G>C MANE Select	NP_068812.1:n.430-10925G>C