Canonical Allele Identifier: CA6475674

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20898465C>G , CM000674.2:g.20898465C>G	GRCh38
NC_000012.11:g.21051399C>G , CM000674.1:g.21051399C>G	GRCh37
NC_000012.10:g.20942666C>G	NCBI36
NG_032071.1:g.92762C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381545.8:c.1712C>G (SLCO1B3) MANE Select	ENSP00000370956.4:p.Ala571Gly
ENST00000261196.6:c.1712C>G (SLCO1B3)	ENSP00000261196.2:p.Ala571Gly
ENST00000381541.7:c.359+39894C>G (SLCO1B3-SLCO1B7)	ENSP00000370952.3:n.359+39894C>G
ENST00000381545.7:c.1712C>G (SLCO1B3)	ENSP00000370956.3:p.Ala571Gly
ENST00000540229.1:c.1712C>G (SLCO1B3-SLCO1B7)	ENSP00000441269.1:p.Ala571Gly
ENST00000544370.1:c.1184C>G (SLCO1B3)	ENSP00000443225.1:p.Ala395Gly
NM_019844.3:c.1712C>G (SLCO1B3)	NP_062818.1:p.Ala571Gly
NM_001349920.1:c.1628C>G (SLCO1B3)	NP_001336849.1:p.Ala543Gly
NM_001349920.2:c.1628C>G (SLCO1B3)	NP_001336849.1:p.Ala543Gly
NM_001371097.1:c.1712C>G (SLCO1B3-SLCO1B7)	NP_001358026.1:p.Ala571Gly
NM_019844.4:c.1712C>G (SLCO1B3) MANE Select	NP_062818.1:p.Ala571Gly