Canonical Allele Identifier: CA2020843387

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20858476A= , CM000674.2:g.20858476A=	GRCh38
NC_000012.11:g.21011410A= , CM000674.1:g.21011410A=	GRCh37
NC_000012.10:g.20902677A=	NCBI36
NG_032071.1:g.52773A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381545.8:c.264A= (SLCO1B3) MANE Select	ENSP00000370956.4:p.Gly88=
ENST00000261196.6:c.264A= (SLCO1B3)	ENSP00000261196.2:p.Gly88=
ENST00000381541.7:c.264A= (SLCO1B3-SLCO1B7)	ENSP00000370952.3:p.Gly88=
ENST00000381545.7:c.264A= (SLCO1B3)	ENSP00000370956.3:p.Gly88=
ENST00000540229.1:c.264A= (SLCO1B3-SLCO1B7)	ENSP00000441269.1:p.Gly88=
ENST00000540853.5:c.264A= (SLCO1B3)	ENSP00000442000.1:p.Gly88=
ENST00000545880.1:n.116A= (SLCO1B3)
NM_019844.3:c.264A= (SLCO1B3)	NP_062818.1:p.Gly88=
NM_001349920.1:c.180A= (SLCO1B3)	NP_001336849.1:p.Gly60=
NM_001349920.2:c.180A= (SLCO1B3)	NP_001336849.1:p.Gly60=
NM_001371097.1:c.264A= (SLCO1B3-SLCO1B7)	NP_001358026.1:p.Gly88=
NM_019844.4:c.264A= (SLCO1B3) MANE Select	NP_062818.1:p.Gly88=