Canonical Allele Identifier: CA2843289322

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20864769C>A , CM000674.2:g.20864769C>A	GRCh38
NC_000012.11:g.21017703C>A , CM000674.1:g.21017703C>A	GRCh37
NC_000012.10:g.20908970C>A	NCBI36
NG_032071.1:g.59066C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381545.8:c.727+1915C>A (SLCO1B3) MANE Select	ENSP00000370956.4:n.727+1915C>A
ENST00000261196.6:c.727+1915C>A (SLCO1B3)	ENSP00000261196.2:n.727+1915C>A
ENST00000381541.7:c.359+6198C>A (SLCO1B3-SLCO1B7)	ENSP00000370952.3:n.359+6198C>A
ENST00000381545.7:c.727+1915C>A (SLCO1B3)	ENSP00000370956.3:n.727+1915C>A
ENST00000540229.1:c.727+1915C>A (SLCO1B3-SLCO1B7)	ENSP00000441269.1:n.727+1915C>A
ENST00000540853.5:c.727+1915C>A (SLCO1B3)	ENSP00000442000.1:n.727+1915C>A
ENST00000544370.1:c.199+1915C>A (SLCO1B3)	ENSP00000443225.1:n.199+1915C>A
NM_019844.3:c.727+1915C>A (SLCO1B3)	NP_062818.1:n.727+1915C>A
NM_001349920.1:c.643+1915C>A (SLCO1B3)	NP_001336849.1:n.643+1915C>A
NM_001349920.2:c.643+1915C>A (SLCO1B3)	NP_001336849.1:n.643+1915C>A
NM_001371097.1:c.727+1915C>A (SLCO1B3-SLCO1B7)	NP_001358026.1:n.727+1915C>A
NM_019844.4:c.727+1915C>A (SLCO1B3) MANE Select	NP_062818.1:n.727+1915C>A