Canonical Allele Identifier: CA478855038
Gene: SLCO1B3 HGNC NCBI
SLCO1B3-SLCO1B7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21015784T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20862850T>C , CM000674.2:g.20862850T>C GRCh38
NC_000012.11:g.21015784T>C , CM000674.1:g.21015784T>C GRCh37
NC_000012.10:g.20907051T>C NCBI36
NG_032071.1:g.57147T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000381545.8:c.723T>C (SLCO1B3) MANE Select ENSP00000370956.4:p.Asp241=
ENST00000261196.6:c.723T>C (SLCO1B3) ENSP00000261196.2:p.Asp241=
ENST00000381541.7:c.359+4279T>C (SLCO1B3-SLCO1B7) ENSP00000370952.3:n.359+4279T>C
ENST00000381545.7:c.723T>C (SLCO1B3) ENSP00000370956.3:p.Asp241=
ENST00000540229.1:c.723T>C (SLCO1B3-SLCO1B7) ENSP00000441269.1:p.Asp241=
ENST00000540853.5:c.723T>C (SLCO1B3) ENSP00000442000.1:p.Asp241=
ENST00000544370.1:c.195T>C (SLCO1B3) ENSP00000443225.1:p.Asp65=
NM_019844.3:c.723T>C (SLCO1B3) NP_062818.1:p.Asp241=
NM_001349920.1:c.639T>C (SLCO1B3) NP_001336849.1:p.Asp213=
NM_001349920.2:c.639T>C (SLCO1B3) NP_001336849.1:p.Asp213=
NM_001371097.1:c.723T>C (SLCO1B3-SLCO1B7) NP_001358026.1:p.Asp241=
NM_019844.4:c.723T>C (SLCO1B3) MANE Select NP_062818.1:p.Asp241=