Canonical Allele Identifier: CA6475522

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20879613T>C , CM000674.2:g.20879613T>C	GRCh38
NC_000012.11:g.21032547T>C , CM000674.1:g.21032547T>C	GRCh37
NC_000012.10:g.20923814T>C	NCBI36
NG_032071.1:g.73910T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381545.8:c.1313T>C (SLCO1B3) MANE Select	ENSP00000370956.4:p.Leu438Pro
ENST00000261196.6:c.1313T>C (SLCO1B3)	ENSP00000261196.2:p.Leu438Pro
ENST00000381541.7:c.359+21042T>C (SLCO1B3-SLCO1B7)	ENSP00000370952.3:n.359+21042T>C
ENST00000381545.7:c.1313T>C (SLCO1B3)	ENSP00000370956.3:p.Leu438Pro
ENST00000540229.1:c.1313T>C (SLCO1B3-SLCO1B7)	ENSP00000441269.1:p.Leu438Pro
ENST00000544370.1:c.785T>C (SLCO1B3)	ENSP00000443225.1:p.Leu262Pro
NM_019844.3:c.1313T>C (SLCO1B3)	NP_062818.1:p.Leu438Pro
NM_001349920.1:c.1229T>C (SLCO1B3)	NP_001336849.1:p.Leu410Pro
NM_001349920.2:c.1229T>C (SLCO1B3)	NP_001336849.1:p.Leu410Pro
NM_001371097.1:c.1313T>C (SLCO1B3-SLCO1B7)	NP_001358026.1:p.Leu438Pro
NM_019844.4:c.1313T>C (SLCO1B3) MANE Select	NP_062818.1:p.Leu438Pro