Canonical Allele Identifier: CA1676973971

Gene: SLC22A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160247269A= , CM000668.2:g.160247269A=	GRCh38
NC_000006.11:g.160668301A= , CM000668.1:g.160668301A=	GRCh37
NC_000006.10:g.160588291A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000366953.8:c.872T= MANE Select	ENSP00000355920.3:p.Ile291=
ENST00000366952.1:c.809T=	ENSP00000355919.1:p.Ile270=
ENST00000366953.7:c.872T=	ENSP00000355920.3:p.Ile291=
ENST00000491092.1:n.769T=
NM_003058.3:c.872T=	NP_003049.2:p.Ile291=
NM_003058.4:c.872T= MANE Select	NP_003049.2:p.Ile291=