Canonical Allele Identifier: CA478855033
Gene: SLCO1B3 HGNC NCBI
SLCO1B3-SLCO1B7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21015775A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20862841A>T , CM000674.2:g.20862841A>T GRCh38
NC_000012.11:g.21015775A>T , CM000674.1:g.21015775A>T GRCh37
NC_000012.10:g.20907042A>T NCBI36
NG_032071.1:g.57138A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381545.8:c.714A>T (SLCO1B3) MANE Select ENSP00000370956.4:p.Gly238=
ENST00000261196.6:c.714A>T (SLCO1B3) ENSP00000261196.2:p.Gly238=
ENST00000381541.7:c.359+4270A>T (SLCO1B3-SLCO1B7) ENSP00000370952.3:n.359+4270A>T
ENST00000381545.7:c.714A>T (SLCO1B3) ENSP00000370956.3:p.Gly238=
ENST00000540229.1:c.714A>T (SLCO1B3-SLCO1B7) ENSP00000441269.1:p.Gly238=
ENST00000540853.5:c.714A>T (SLCO1B3) ENSP00000442000.1:p.Gly238=
ENST00000544370.1:c.186A>T (SLCO1B3) ENSP00000443225.1:p.Gly62=
NM_019844.3:c.714A>T (SLCO1B3) NP_062818.1:p.Gly238=
NM_001349920.1:c.630A>T (SLCO1B3) NP_001336849.1:p.Gly210=
NM_001349920.2:c.630A>T (SLCO1B3) NP_001336849.1:p.Gly210=
NM_001371097.1:c.714A>T (SLCO1B3-SLCO1B7) NP_001358026.1:p.Gly238=
NM_019844.4:c.714A>T (SLCO1B3) MANE Select NP_062818.1:p.Gly238=