Canonical Allele Identifier: CA2020843377
Gene: SLCO1B3 HGNC NCBI
SLCO1B3-SLCO1B7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20858446G= , CM000674.2:g.20858446G= GRCh38
NC_000012.11:g.21011380G= , CM000674.1:g.21011380G= GRCh37
NC_000012.10:g.20902647G= NCBI36
NG_032071.1:g.52743G=

Transcript Alleles

HGVS Amino-acid change
ENST00000381545.8:c.234G= (SLCO1B3) MANE Select ENSP00000370956.4:p.Leu78=
ENST00000261196.6:c.234G= (SLCO1B3) ENSP00000261196.2:p.Leu78=
ENST00000381541.7:c.234G= (SLCO1B3-SLCO1B7) ENSP00000370952.3:p.Leu78=
ENST00000381545.7:c.234G= (SLCO1B3) ENSP00000370956.3:p.Leu78=
ENST00000540229.1:c.234G= (SLCO1B3-SLCO1B7) ENSP00000441269.1:p.Leu78=
ENST00000540853.5:c.234G= (SLCO1B3) ENSP00000442000.1:p.Leu78=
ENST00000545880.1:n.86G= (SLCO1B3)
NM_019844.3:c.234G= (SLCO1B3) NP_062818.1:p.Leu78=
NM_001349920.1:c.150G= (SLCO1B3) NP_001336849.1:p.Leu50=
NM_001349920.2:c.150G= (SLCO1B3) NP_001336849.1:p.Leu50=
NM_001371097.1:c.234G= (SLCO1B3-SLCO1B7) NP_001358026.1:p.Leu78=
NM_019844.4:c.234G= (SLCO1B3) MANE Select NP_062818.1:p.Leu78=