Canonical Allele Identifier: CA6475610

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20883477A>G , CM000674.2:g.20883477A>G	GRCh38
NC_000012.11:g.21036411A>G , CM000674.1:g.21036411A>G	GRCh37
NC_000012.10:g.20927678A>G	NCBI36
NG_032071.1:g.77774A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381545.8:c.1557A>G (SLCO1B3) MANE Select	ENSP00000370956.4:p.Ala519=
ENST00000261196.6:c.1557A>G (SLCO1B3)	ENSP00000261196.2:p.Ala519=
ENST00000381541.7:c.359+24906A>G (SLCO1B3-SLCO1B7)	ENSP00000370952.3:n.359+24906A>G
ENST00000381545.7:c.1557A>G (SLCO1B3)	ENSP00000370956.3:p.Ala519=
ENST00000540229.1:c.1557A>G (SLCO1B3-SLCO1B7)	ENSP00000441269.1:p.Ala519=
ENST00000544370.1:c.1029A>G (SLCO1B3)	ENSP00000443225.1:p.Ala343=
NM_019844.3:c.1557A>G (SLCO1B3)	NP_062818.1:p.Ala519=
NM_001349920.1:c.1473A>G (SLCO1B3)	NP_001336849.1:p.Ala491=
NM_001349920.2:c.1473A>G (SLCO1B3)	NP_001336849.1:p.Ala491=
NM_001371097.1:c.1557A>G (SLCO1B3-SLCO1B7)	NP_001358026.1:p.Ala519=
NM_019844.4:c.1557A>G (SLCO1B3) MANE Select	NP_062818.1:p.Ala519=