Canonical Allele Identifier: CA384092293

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Linked Data

• gnomAD v4: 12-20862828-A-G
• MyVariant Identifiers: chr12:g.21015762A>G (hg19) ; chr12:g.20862828A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20862828A>G , CM000674.2:g.20862828A>G	GRCh38
NC_000012.11:g.21015762A>G , CM000674.1:g.21015762A>G	GRCh37
NC_000012.10:g.20907029A>G	NCBI36
NG_032071.1:g.57125A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381545.8:c.701A>G (SLCO1B3) MANE Select	ENSP00000370956.4:p.Tyr234Cys
ENST00000261196.6:c.701A>G (SLCO1B3)	ENSP00000261196.2:p.Tyr234Cys
ENST00000381541.7:c.359+4257A>G (SLCO1B3-SLCO1B7)	ENSP00000370952.3:n.359+4257A>G
ENST00000381545.7:c.701A>G (SLCO1B3)	ENSP00000370956.3:p.Tyr234Cys
ENST00000540229.1:c.701A>G (SLCO1B3-SLCO1B7)	ENSP00000441269.1:p.Tyr234Cys
ENST00000540853.5:c.701A>G (SLCO1B3)	ENSP00000442000.1:p.Tyr234Cys
ENST00000544370.1:c.173A>G (SLCO1B3)	ENSP00000443225.1:p.Tyr58Cys
NM_019844.3:c.701A>G (SLCO1B3)	NP_062818.1:p.Tyr234Cys
NM_001349920.1:c.617A>G (SLCO1B3)	NP_001336849.1:p.Tyr206Cys
NM_001349920.2:c.617A>G (SLCO1B3)	NP_001336849.1:p.Tyr206Cys
NM_001371097.1:c.701A>G (SLCO1B3-SLCO1B7)	NP_001358026.1:p.Tyr234Cys
NM_019844.4:c.701A>G (SLCO1B3) MANE Select	NP_062818.1:p.Tyr234Cys