Canonical Allele Identifier: CA6475784

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20916115G>A , CM000674.2:g.20916115G>A	GRCh38
NC_000012.11:g.21069049G>A , CM000674.1:g.21069049G>A	GRCh37
NC_000012.10:g.20960316G>A	NCBI36
NG_032071.1:g.110412G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381545.8:c.1977G>A (SLCO1B3) MANE Select	ENSP00000370956.4:p.Ser659=
ENST00000261196.6:c.1977G>A (SLCO1B3)	ENSP00000261196.2:p.Ser659=
ENST00000381541.7:c.359+57544G>A (SLCO1B3-SLCO1B7)	ENSP00000370952.3:n.359+57544G>A
ENST00000381545.7:c.1977G>A (SLCO1B3)	ENSP00000370956.3:p.Ser659=
ENST00000540229.1:c.1865+14648G>A (SLCO1B3-SLCO1B7)	ENSP00000441269.1:n.1865+14648G>A
NM_019844.3:c.1977G>A (SLCO1B3)	NP_062818.1:p.Ser659=
NM_001349920.1:c.1893G>A (SLCO1B3)	NP_001336849.1:p.Ser631=
NM_001349920.2:c.1893G>A (SLCO1B3)	NP_001336849.1:p.Ser631=
NM_001371097.1:c.1865+14648G>A (SLCO1B3-SLCO1B7)	NP_001358026.1:n.1865+14648G>A
NM_019844.4:c.1977G>A (SLCO1B3) MANE Select	NP_062818.1:p.Ser659=