Canonical Allele Identifier: CA1096526355
Gene: SLC22A2 HGNC NCBI

Linked Data

dbSNP Id: rs1783141057

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160249097T>C , CM000668.2:g.160249097T>C GRCh38
NC_000006.11:g.160670129T>C , CM000668.1:g.160670129T>C GRCh37
NC_000006.10:g.160590119T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366953.8:c.842+119A>G MANE Select ENSP00000355920.3:n.842+119A>G
ENST00000366952.1:c.779+119A>G ENSP00000355919.1:n.779+119A>G
ENST00000366953.7:c.842+119A>G ENSP00000355920.3:n.842+119A>G
ENST00000491092.1:n.739+119A>G
NM_003058.3:c.842+119A>G NP_003049.2:n.842+119A>G
NM_003058.4:c.842+119A>G MANE Select NP_003049.2:n.842+119A>G