Canonical Allele Identifier: CA2713607137
Gene: SLC22A2 HGNC NCBI

Linked Data

dbSNP Id: rs2114868430

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160249155C>T , CM000668.2:g.160249155C>T GRCh38
NC_000006.11:g.160670187C>T , CM000668.1:g.160670187C>T GRCh37
NC_000006.10:g.160590177C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366953.8:c.842+61G>A MANE Select ENSP00000355920.3:n.842+61G>A
ENST00000366952.1:c.779+61G>A ENSP00000355919.1:n.779+61G>A
ENST00000366953.7:c.842+61G>A ENSP00000355920.3:n.842+61G>A
ENST00000491092.1:n.739+61G>A
NM_003058.3:c.842+61G>A NP_003049.2:n.842+61G>A
NM_003058.4:c.842+61G>A MANE Select NP_003049.2:n.842+61G>A