Canonical Allele Identifier: CA384092054

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Linked Data

• MyVariant Identifiers: chr12:g.21015693G>C (hg19) ; chr12:g.20862759G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20862759G>C , CM000674.2:g.20862759G>C	GRCh38
NC_000012.11:g.21015693G>C , CM000674.1:g.21015693G>C	GRCh37
NC_000012.10:g.20906960G>C	NCBI36
NG_032071.1:g.57056G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381545.8:c.632G>C (SLCO1B3) MANE Select	ENSP00000370956.4:p.Ser211Thr
ENST00000261196.6:c.632G>C (SLCO1B3)	ENSP00000261196.2:p.Ser211Thr
ENST00000381541.7:c.359+4188G>C (SLCO1B3-SLCO1B7)	ENSP00000370952.3:n.359+4188G>C
ENST00000381545.7:c.632G>C (SLCO1B3)	ENSP00000370956.3:p.Ser211Thr
ENST00000540229.1:c.632G>C (SLCO1B3-SLCO1B7)	ENSP00000441269.1:p.Ser211Thr
ENST00000540853.5:c.632G>C (SLCO1B3)	ENSP00000442000.1:p.Ser211Thr
ENST00000544370.1:c.104G>C (SLCO1B3)	ENSP00000443225.1:p.Ser35Thr
NM_019844.3:c.632G>C (SLCO1B3)	NP_062818.1:p.Ser211Thr
NM_001349920.1:c.548G>C (SLCO1B3)	NP_001336849.1:p.Ser183Thr
NM_001349920.2:c.548G>C (SLCO1B3)	NP_001336849.1:p.Ser183Thr
NM_001371097.1:c.632G>C (SLCO1B3-SLCO1B7)	NP_001358026.1:p.Ser211Thr
NM_019844.4:c.632G>C (SLCO1B3) MANE Select	NP_062818.1:p.Ser211Thr