Canonical Allele Identifier: CA2020845859
Gene: SLCO1B3 HGNC NCBI
SLCO1B3-SLCO1B7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20863062_20863063delinsAT , CM000674.2:g.20863062_20863063delinsAT GRCh38
NC_000012.11:g.21015996_21015997delinsAT , CM000674.1:g.21015996_21015997delinsAT GRCh37
NC_000012.10:g.20907263_20907264delinsAT NCBI36
NG_032071.1:g.57359_57360delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000381545.8:c.727+208_727+209delinsAT (SLCO1B3) MANE Select ENSP00000370956.4:n.727+208_727+209delins...
ENST00000261196.6:c.727+208_727+209delinsAT (SLCO1B3) ENSP00000261196.2:n.727+208_727+209delins...
ENST00000381541.7:c.359+4491_359+4492delinsAT (SLCO1B3-SLCO1B7) ENSP00000370952.3:n.359+4491_359+4492deli...
ENST00000381545.7:c.727+208_727+209delinsAT (SLCO1B3) ENSP00000370956.3:n.727+208_727+209delins...
ENST00000540229.1:c.727+208_727+209delinsAT (SLCO1B3-SLCO1B7) ENSP00000441269.1:n.727+208_727+209delins...
ENST00000540853.5:c.727+208_727+209delinsAT (SLCO1B3) ENSP00000442000.1:n.727+208_727+209delins...
ENST00000544370.1:c.199+208_199+209delinsAT (SLCO1B3) ENSP00000443225.1:n.199+208_199+209delins...
NM_019844.3:c.727+208_727+209delinsAT (SLCO1B3) NP_062818.1:n.727+208_727+209delinsAT
NM_001349920.1:c.643+208_643+209delinsAT (SLCO1B3) NP_001336849.1:n.643+208_643+209delinsAT
NM_001349920.2:c.643+208_643+209delinsAT (SLCO1B3) NP_001336849.1:n.643+208_643+209delinsAT
NM_001371097.1:c.727+208_727+209delinsAT (SLCO1B3-SLCO1B7) NP_001358026.1:n.727+208_727+209delinsAT
NM_019844.4:c.727+208_727+209delinsAT (SLCO1B3) MANE Select NP_062818.1:n.727+208_727+209delinsAT
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