Canonical Allele Identifier: CA2020843423

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20858556A= , CM000674.2:g.20858556A=	GRCh38
NC_000012.11:g.21011490A= , CM000674.1:g.21011490A=	GRCh37
NC_000012.10:g.20902757A=	NCBI36
NG_032071.1:g.52853A=

Transcript Alleles

HGVS	Amino-acid Change
NM_019844.4:c.344A= (SLCO1B3) MANE Select	NP_062818.1:p.His115=
ENST00000381545.8:c.344A= (SLCO1B3) MANE Select	ENSP00000370956.4:p.His115=
NM_001349920.1:c.260A= (SLCO1B3)	NP_001336849.1:p.His87=
NM_001349920.2:c.260A= (SLCO1B3)	NP_001336849.1:p.His87=
NM_001371097.1:c.344A= (SLCO1B3-SLCO1B7)	NP_001358026.1:p.His115=
NM_019844.3:c.344A= (SLCO1B3)	NP_062818.1:p.His115=
ENST00000261196.6:c.344A= (SLCO1B3)	ENSP00000261196.2:p.His115=
ENST00000381541.7:c.344A= (SLCO1B3-SLCO1B7)	ENSP00000370952.3:p.His115=
ENST00000381545.7:c.344A= (SLCO1B3)	ENSP00000370956.3:p.His115=
ENST00000540229.1:c.344A= (SLCO1B3-SLCO1B7)	ENSP00000441269.1:p.His115=
ENST00000540853.5:c.344A= (SLCO1B3)	ENSP00000442000.1:p.His115=
ENST00000545880.1:n.196A= (SLCO1B3)