Canonical Allele Identifier: CA384099114

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Linked Data

• MyVariant Identifiers: chr12:g.21011462A>C (hg19) ; chr12:g.20858528A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20858528A>C , CM000674.2:g.20858528A>C	GRCh38
NC_000012.11:g.21011462A>C , CM000674.1:g.21011462A>C	GRCh37
NC_000012.10:g.20902729A>C	NCBI36
NG_032071.1:g.52825A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381545.8:c.316A>C (SLCO1B3) MANE Select	ENSP00000370956.4:p.Thr106Pro
ENST00000261196.6:c.316A>C (SLCO1B3)	ENSP00000261196.2:p.Thr106Pro
ENST00000381541.7:c.316A>C (SLCO1B3-SLCO1B7)	ENSP00000370952.3:p.Thr106Pro
ENST00000381545.7:c.316A>C (SLCO1B3)	ENSP00000370956.3:p.Thr106Pro
ENST00000540229.1:c.316A>C (SLCO1B3-SLCO1B7)	ENSP00000441269.1:p.Thr106Pro
ENST00000540853.5:c.316A>C (SLCO1B3)	ENSP00000442000.1:p.Thr106Pro
ENST00000545880.1:n.168A>C (SLCO1B3)
NM_019844.3:c.316A>C (SLCO1B3)	NP_062818.1:p.Thr106Pro
NM_001349920.1:c.232A>C (SLCO1B3)	NP_001336849.1:p.Thr78Pro
NM_001349920.2:c.232A>C (SLCO1B3)	NP_001336849.1:p.Thr78Pro
NM_001371097.1:c.316A>C (SLCO1B3-SLCO1B7)	NP_001358026.1:p.Thr106Pro
NM_019844.4:c.316A>C (SLCO1B3) MANE Select	NP_062818.1:p.Thr106Pro