Canonical Allele Identifier: CA478854977

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Linked Data

• dbSNP Id: rs1225239618
• gnomAD v2: 12-21015691-T-C
• gnomAD v4: 12-20862757-T-C
• MyVariant Identifiers: chr12:g.21015691T>C (hg19) ; chr12:g.20862757T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20862757T>C , CM000674.2:g.20862757T>C	GRCh38
NC_000012.11:g.21015691T>C , CM000674.1:g.21015691T>C	GRCh37
NC_000012.10:g.20906958T>C	NCBI36
NG_032071.1:g.57054T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381545.8:c.630T>C (SLCO1B3) MANE Select	ENSP00000370956.4:p.Gly210=
ENST00000261196.6:c.630T>C (SLCO1B3)	ENSP00000261196.2:p.Gly210=
ENST00000381541.7:c.359+4186T>C (SLCO1B3-SLCO1B7)	ENSP00000370952.3:n.359+4186T>C
ENST00000381545.7:c.630T>C (SLCO1B3)	ENSP00000370956.3:p.Gly210=
ENST00000540229.1:c.630T>C (SLCO1B3-SLCO1B7)	ENSP00000441269.1:p.Gly210=
ENST00000540853.5:c.630T>C (SLCO1B3)	ENSP00000442000.1:p.Gly210=
ENST00000544370.1:c.102T>C (SLCO1B3)	ENSP00000443225.1:p.Gly34=
NM_019844.3:c.630T>C (SLCO1B3)	NP_062818.1:p.Gly210=
NM_001349920.1:c.546T>C (SLCO1B3)	NP_001336849.1:p.Gly182=
NM_001349920.2:c.546T>C (SLCO1B3)	NP_001336849.1:p.Gly182=
NM_001371097.1:c.630T>C (SLCO1B3-SLCO1B7)	NP_001358026.1:p.Gly210=
NM_019844.4:c.630T>C (SLCO1B3) MANE Select	NP_062818.1:p.Gly210=