Canonical Allele Identifier: CA2836010283

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20892508A>T , CM000674.2:g.20892508A>T	GRCh38
NC_000012.11:g.21045442A>T , CM000674.1:g.21045442A>T	GRCh37
NC_000012.10:g.20936709A>T	NCBI36
NG_032071.1:g.86805A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381545.8:c.1683-5928A>T (SLCO1B3) MANE Select	ENSP00000370956.4:n.1683-5928A>T
ENST00000261196.6:c.1683-5928A>T (SLCO1B3)	ENSP00000261196.2:n.1683-5928A>T
ENST00000381541.7:c.359+33937A>T (SLCO1B3-SLCO1B7)	ENSP00000370952.3:n.359+33937A>T
ENST00000381545.7:c.1683-5928A>T (SLCO1B3)	ENSP00000370956.3:n.1683-5928A>T
ENST00000540229.1:c.1683-5928A>T (SLCO1B3-SLCO1B7)	ENSP00000441269.1:n.1683-5928A>T
ENST00000544370.1:c.1155-5928A>T (SLCO1B3)	ENSP00000443225.1:n.1155-5928A>T
NM_019844.3:c.1683-5928A>T (SLCO1B3)	NP_062818.1:n.1683-5928A>T
NM_001349920.1:c.1599-5928A>T (SLCO1B3)	NP_001336849.1:n.1599-5928A>T
NM_001349920.2:c.1599-5928A>T (SLCO1B3)	NP_001336849.1:n.1599-5928A>T
NM_001371097.1:c.1683-5928A>T (SLCO1B3-SLCO1B7)	NP_001358026.1:n.1683-5928A>T
NM_019844.4:c.1683-5928A>T (SLCO1B3) MANE Select	NP_062818.1:n.1683-5928A>T