Canonical Allele Identifier: CA478854982
Gene: SLCO1B3 HGNC NCBI
SLCO1B3-SLCO1B7 HGNC NCBI

Linked Data

dbSNP Id: rs778412645
MyVariant Identifiers: chr12:g.21015703A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20862769A>G , CM000674.2:g.20862769A>G GRCh38
NC_000012.11:g.21015703A>G , CM000674.1:g.21015703A>G GRCh37
NC_000012.10:g.20906970A>G NCBI36
NG_032071.1:g.57066A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381545.8:c.642A>G (SLCO1B3) MANE Select ENSP00000370956.4:p.Ala214=
ENST00000261196.6:c.642A>G (SLCO1B3) ENSP00000261196.2:p.Ala214=
ENST00000381541.7:c.359+4198A>G (SLCO1B3-SLCO1B7) ENSP00000370952.3:n.359+4198A>G
ENST00000381545.7:c.642A>G (SLCO1B3) ENSP00000370956.3:p.Ala214=
ENST00000540229.1:c.642A>G (SLCO1B3-SLCO1B7) ENSP00000441269.1:p.Ala214=
ENST00000540853.5:c.642A>G (SLCO1B3) ENSP00000442000.1:p.Ala214=
ENST00000544370.1:c.114A>G (SLCO1B3) ENSP00000443225.1:p.Ala38=
NM_019844.3:c.642A>G (SLCO1B3) NP_062818.1:p.Ala214=
NM_001349920.1:c.558A>G (SLCO1B3) NP_001336849.1:p.Ala186=
NM_001349920.2:c.558A>G (SLCO1B3) NP_001336849.1:p.Ala186=
NM_001371097.1:c.642A>G (SLCO1B3-SLCO1B7) NP_001358026.1:p.Ala214=
NM_019844.4:c.642A>G (SLCO1B3) MANE Select NP_062818.1:p.Ala214=