Canonical Allele Identifier: CA2713498998
Gene: SLC22A2 HGNC NCBI

Linked Data

dbSNP Id: rs752462661

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160249189T>A , CM000668.2:g.160249189T>A GRCh38
NC_000006.11:g.160670221T>A , CM000668.1:g.160670221T>A GRCh37
NC_000006.10:g.160590211T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366953.8:c.842+27A>T MANE Select ENSP00000355920.3:n.842+27A>T
ENST00000366952.1:c.779+27A>T ENSP00000355919.1:n.779+27A>T
ENST00000366953.7:c.842+27A>T ENSP00000355920.3:n.842+27A>T
ENST00000491092.1:n.739+27A>T
NM_003058.3:c.842+27A>T NP_003049.2:n.842+27A>T
NM_003058.4:c.842+27A>T MANE Select NP_003049.2:n.842+27A>T