Canonical Allele Identifier: CA366345732

Gene: SLC22A3

Linked Data

• MyVariant Identifiers: chr6:g.160857903T>C (hg19) ; chr6:g.160436871T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160436871T>C , CM000668.2:g.160436871T>C	GRCh38
NC_000006.11:g.160857903T>C , CM000668.1:g.160857903T>C	GRCh37
NC_000006.10:g.160777893T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1067T>C MANE Select	ENSP00000275300.2:p.Phe356Ser
ENST00000275300.2:c.1067T>C	ENSP00000275300.2:p.Phe356Ser
NM_021977.3:c.1067T>C	NP_068812.1:p.Phe356Ser
XM_005267106.3:c.674T>C	XP_005267163.1:p.Phe225Ser
XM_011536075.1:c.611T>C	XP_011534377.1:p.Phe204Ser
XM_011536076.1:c.611T>C	XP_011534378.1:p.Phe204Ser
XM_011536077.1:c.611T>C	XP_011534379.1:p.Phe204Ser
XR_245546.1:n.1018-5890T>C
XM_005267106.5:c.674T>C	XP_005267163.1:p.Phe225Ser
XM_011536075.2:c.611T>C	XP_011534377.1:p.Phe204Ser
XM_011536076.3:c.611T>C	XP_011534378.1:p.Phe204Ser
XM_017011203.2:c.611T>C	XP_016866692.1:p.Phe204Ser
XR_001743588.1:n.1018-126T>C
XR_001743589.1:n.1018-5890T>C
NM_021977.4:c.1067T>C MANE Select	NP_068812.1:p.Phe356Ser