Canonical Allele Identifier: CA384092335

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Linked Data

• MyVariant Identifiers: chr12:g.21015783A>C (hg19) ; chr12:g.20862849A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20862849A>C , CM000674.2:g.20862849A>C	GRCh38
NC_000012.11:g.21015783A>C , CM000674.1:g.21015783A>C	GRCh37
NC_000012.10:g.20907050A>C	NCBI36
NG_032071.1:g.57146A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000381545.8:c.722A>C (SLCO1B3) MANE Select	ENSP00000370956.4:p.Asp241Ala
ENST00000261196.6:c.722A>C (SLCO1B3)	ENSP00000261196.2:p.Asp241Ala
ENST00000381541.7:c.359+4278A>C (SLCO1B3-SLCO1B7)	ENSP00000370952.3:n.359+4278A>C
ENST00000381545.7:c.722A>C (SLCO1B3)	ENSP00000370956.3:p.Asp241Ala
ENST00000540229.1:c.722A>C (SLCO1B3-SLCO1B7)	ENSP00000441269.1:p.Asp241Ala
ENST00000540853.5:c.722A>C (SLCO1B3)	ENSP00000442000.1:p.Asp241Ala
ENST00000544370.1:c.194A>C (SLCO1B3)	ENSP00000443225.1:p.Asp65Ala
NM_019844.3:c.722A>C (SLCO1B3)	NP_062818.1:p.Asp241Ala
NM_001349920.1:c.638A>C (SLCO1B3)	NP_001336849.1:p.Asp213Ala
NM_001349920.2:c.638A>C (SLCO1B3)	NP_001336849.1:p.Asp213Ala
NM_001371097.1:c.722A>C (SLCO1B3-SLCO1B7)	NP_001358026.1:p.Asp241Ala
NM_019844.4:c.722A>C (SLCO1B3) MANE Select	NP_062818.1:p.Asp241Ala