Canonical Allele Identifier: CA384092315

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Linked Data

• dbSNP Id: rs1446729548
• gnomAD v2: 12-21015772-T-G
• gnomAD v4: 12-20862838-T-G
• MyVariant Identifiers: chr12:g.21015772T>G (hg19) ; chr12:g.20862838T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20862838T>G , CM000674.2:g.20862838T>G	GRCh38
NC_000012.11:g.21015772T>G , CM000674.1:g.21015772T>G	GRCh37
NC_000012.10:g.20907039T>G	NCBI36
NG_032071.1:g.57135T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381545.8:c.711T>G (SLCO1B3) MANE Select	ENSP00000370956.4:p.Ile237Met
ENST00000261196.6:c.711T>G (SLCO1B3)	ENSP00000261196.2:p.Ile237Met
ENST00000381541.7:c.359+4267T>G (SLCO1B3-SLCO1B7)	ENSP00000370952.3:n.359+4267T>G
ENST00000381545.7:c.711T>G (SLCO1B3)	ENSP00000370956.3:p.Ile237Met
ENST00000540229.1:c.711T>G (SLCO1B3-SLCO1B7)	ENSP00000441269.1:p.Ile237Met
ENST00000540853.5:c.711T>G (SLCO1B3)	ENSP00000442000.1:p.Ile237Met
ENST00000544370.1:c.183T>G (SLCO1B3)	ENSP00000443225.1:p.Ile61Met
NM_019844.3:c.711T>G (SLCO1B3)	NP_062818.1:p.Ile237Met
NM_001349920.1:c.627T>G (SLCO1B3)	NP_001336849.1:p.Ile209Met
NM_001349920.2:c.627T>G (SLCO1B3)	NP_001336849.1:p.Ile209Met
NM_001371097.1:c.711T>G (SLCO1B3-SLCO1B7)	NP_001358026.1:p.Ile237Met
NM_019844.4:c.711T>G (SLCO1B3) MANE Select	NP_062818.1:p.Ile237Met