Canonical Allele Identifier: CA6475135
Gene: SLCO1B3 HGNC NCBI
SLCO1B3-SLCO1B7 HGNC NCBI

Linked Data

ClinVar Variation Id: 261184
dbSNP Id: rs4149117

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20858546T>G , CM000674.2:g.20858546T>G GRCh38
NC_000012.11:g.21011480T>G , CM000674.1:g.21011480T>G GRCh37
NC_000012.10:g.20902747T>G NCBI36
NG_032071.1:g.52843T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000381545.8:c.334T>G (SLCO1B3) MANE Select ENSP00000370956.4:p.Ser112Ala
ENST00000261196.6:c.334T>G (SLCO1B3) ENSP00000261196.2:p.Ser112Ala
ENST00000381541.7:c.334T>G (SLCO1B3-SLCO1B7) ENSP00000370952.3:p.Ser112Ala
ENST00000381545.7:c.334T>G (SLCO1B3) ENSP00000370956.3:p.Ser112Ala
ENST00000540229.1:c.334T>G (SLCO1B3-SLCO1B7) ENSP00000441269.1:p.Ser112Ala
ENST00000540853.5:c.334T>G (SLCO1B3) ENSP00000442000.1:p.Ser112Ala
ENST00000545880.1:n.186T>G (SLCO1B3)
NM_019844.3:c.334T>G (SLCO1B3) NP_062818.1:p.Ser112Ala
NM_001349920.1:c.250T>G (SLCO1B3) NP_001336849.1:p.Ser84Ala
NM_001349920.2:c.250T>G (SLCO1B3) NP_001336849.1:p.Ser84Ala
NM_001371097.1:c.334T>G (SLCO1B3-SLCO1B7) NP_001358026.1:p.Ser112Ala
NM_019844.4:c.334T>G (SLCO1B3) MANE Select NP_062818.1:p.Ser112Ala