Canonical Allele Identifier: CA2977635295

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20879358dup , CM000674.2:g.20879358dup	GRCh38
NC_000012.11:g.21032292dup , CM000674.1:g.21032292dup	GRCh37
NC_000012.10:g.20923559dup	NCBI36
NG_032071.1:g.73655dup

Transcript Alleles

HGVS	Amino-acid Change
NM_019844.4:c.1136-78dup (SLCO1B3) MANE Select	NP_062818.1:n.1136-78dup
ENST00000381545.8:c.1136-78dup (SLCO1B3) MANE Select	ENSP00000370956.4:n.1136-78dup
NM_001349920.1:c.1052-78dup (SLCO1B3)	NP_001336849.1:n.1052-78dup
NM_001349920.2:c.1052-78dup (SLCO1B3)	NP_001336849.1:n.1052-78dup
NM_001371097.1:c.1136-78dup (SLCO1B3-SLCO1B7)	NP_001358026.1:n.1136-78dup
NM_019844.3:c.1136-78dup (SLCO1B3)	NP_062818.1:n.1136-78dup
ENST00000261196.6:c.1136-78dup (SLCO1B3)	ENSP00000261196.2:n.1136-78dup
ENST00000381541.7:c.359+20787dup (SLCO1B3-SLCO1B7)	ENSP00000370952.3:n.359+20787dup
ENST00000381545.7:c.1136-78dup (SLCO1B3)	ENSP00000370956.3:n.1136-78dup
ENST00000540229.1:c.1136-78dup (SLCO1B3-SLCO1B7)	ENSP00000441269.1:n.1136-78dup
ENST00000544370.1:c.608-78dup (SLCO1B3)	ENSP00000443225.1:n.608-78dup