Canonical Allele Identifier: CA2020845709

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Linked Data

• dbSNP Id: rs1865294093

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20862751T>C , CM000674.2:g.20862751T>C	GRCh38
NC_000012.11:g.21015685T>C , CM000674.1:g.21015685T>C	GRCh37
NC_000012.10:g.20906952T>C	NCBI36
NG_032071.1:g.57048T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381545.8:c.629-5T>C (SLCO1B3) MANE Select	ENSP00000370956.4:n.629-5T>C
ENST00000261196.6:c.629-5T>C (SLCO1B3)	ENSP00000261196.2:n.629-5T>C
ENST00000381541.7:c.359+4180T>C (SLCO1B3-SLCO1B7)	ENSP00000370952.3:n.359+4180T>C
ENST00000381545.7:c.629-5T>C (SLCO1B3)	ENSP00000370956.3:n.629-5T>C
ENST00000540229.1:c.629-5T>C (SLCO1B3-SLCO1B7)	ENSP00000441269.1:n.629-5T>C
ENST00000540853.5:c.629-5T>C (SLCO1B3)	ENSP00000442000.1:n.629-5T>C
ENST00000544370.1:c.101-5T>C (SLCO1B3)	ENSP00000443225.1:n.101-5T>C
NM_019844.3:c.629-5T>C (SLCO1B3)	NP_062818.1:n.629-5T>C
NM_001349920.1:c.545-5T>C (SLCO1B3)	NP_001336849.1:n.545-5T>C
NM_001349920.2:c.545-5T>C (SLCO1B3)	NP_001336849.1:n.545-5T>C
NM_001371097.1:c.629-5T>C (SLCO1B3-SLCO1B7)	NP_001358026.1:n.629-5T>C
NM_019844.4:c.629-5T>C (SLCO1B3) MANE Select	NP_062818.1:n.629-5T>C