Canonical Allele Identifier: CA13560564
Gene: SLC22A8 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11231299

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.63003916G>A , CM000673.2:g.63003916G>A GRCh38
NC_000011.9:g.62771388G>A , CM000673.1:g.62771388G>A GRCh37
NC_000011.8:g.62527964G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001184732.1:c.334-3093C>T VV NP_001171661.1:p.=
NM_001184733.1:c.61-3093C>T VV NP_001171662.1:p.=
NM_001184736.1:c.-36-3093C>T VV NP_001171665.1:p.=
NM_004254.3:c.334-3093C>T VV NP_004245.2:p.=
NM_004254.4:c.334-3093C>T VV MANE Preferred
ENST00000311438.12:n.334-3093C>T ENSP00000311463.8:p.=
ENST00000336232.6:c.334-3093C>T ENSP00000337335.2:p.=
ENST00000430500.6:c.334-3093C>T ENSP00000398548.2:p.=
ENST00000535878.5:c.-36-3093C>T ENSP00000443368.1:p.=
ENST00000545207.5:c.61-3093C>T ENSP00000441658.1:p.=