Canonical Allele Identifier: CA2578789348
Gene: SLC22A2 HGNC NCBI

Linked Data

dbSNP Id: rs2114868438

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160249162C>G , CM000668.2:g.160249162C>G GRCh38
NC_000006.11:g.160670194C>G , CM000668.1:g.160670194C>G GRCh37
NC_000006.10:g.160590184C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366953.8:c.842+54G>C MANE Select ENSP00000355920.3:n.842+54G>C
ENST00000366952.1:c.779+54G>C ENSP00000355919.1:n.779+54G>C
ENST00000366953.7:c.842+54G>C ENSP00000355920.3:n.842+54G>C
ENST00000491092.1:n.739+54G>C
NM_003058.3:c.842+54G>C NP_003049.2:n.842+54G>C
NM_003058.4:c.842+54G>C MANE Select NP_003049.2:n.842+54G>C