Canonical Allele Identifier: CA1676973969

Gene: SLC22A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160247262C= , CM000668.2:g.160247262C=	GRCh38
NC_000006.11:g.160668294C= , CM000668.1:g.160668294C=	GRCh37
NC_000006.10:g.160588284C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366953.8:c.879G= MANE Select	ENSP00000355920.3:p.Gln293=
ENST00000366952.1:c.816G=	ENSP00000355919.1:p.Gln272=
ENST00000366953.7:c.879G=	ENSP00000355920.3:p.Gln293=
ENST00000491092.1:n.776G=
NM_003058.3:c.879G=	NP_003049.2:p.Gln293=
NM_003058.4:c.879G= MANE Select	NP_003049.2:p.Gln293=