Canonical Allele Identifier: CA2020846807
Gene: SLCO1B3 HGNC NCBI
SLCO1B3-SLCO1B7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20864890T= , CM000674.2:g.20864890T= GRCh38
NC_000012.11:g.21017824T= , CM000674.1:g.21017824T= GRCh37
NC_000012.10:g.20909091T= NCBI36
NG_032071.1:g.59187T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381545.8:c.727+2036T= (SLCO1B3) MANE Select ENSP00000370956.4:n.727+2036T=
ENST00000261196.6:c.727+2036T= (SLCO1B3) ENSP00000261196.2:n.727+2036T=
ENST00000381541.7:c.359+6319T= (SLCO1B3-SLCO1B7) ENSP00000370952.3:n.359+6319T=
ENST00000381545.7:c.727+2036T= (SLCO1B3) ENSP00000370956.3:n.727+2036T=
ENST00000540229.1:c.727+2036T= (SLCO1B3-SLCO1B7) ENSP00000441269.1:n.727+2036T=
ENST00000540853.5:c.727+2036T= (SLCO1B3) ENSP00000442000.1:n.727+2036T=
ENST00000544370.1:c.199+2036T= (SLCO1B3) ENSP00000443225.1:n.199+2036T=
NM_019844.3:c.727+2036T= (SLCO1B3) NP_062818.1:n.727+2036T=
NM_001349920.1:c.643+2036T= (SLCO1B3) NP_001336849.1:n.643+2036T=
NM_001349920.2:c.643+2036T= (SLCO1B3) NP_001336849.1:n.643+2036T=
NM_001371097.1:c.727+2036T= (SLCO1B3-SLCO1B7) NP_001358026.1:n.727+2036T=
NM_019844.4:c.727+2036T= (SLCO1B3) MANE Select NP_062818.1:n.727+2036T=