Canonical Allele Identifier: CA478862227
Gene: SLCO1B3 HGNC NCBI
SLCO1B3-SLCO1B7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21011488A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20858554A>T , CM000674.2:g.20858554A>T GRCh38
NC_000012.11:g.21011488A>T , CM000674.1:g.21011488A>T GRCh37
NC_000012.10:g.20902755A>T NCBI36
NG_032071.1:g.52851A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381545.8:c.342A>T (SLCO1B3) MANE Select ENSP00000370956.4:p.Pro114=
ENST00000261196.6:c.342A>T (SLCO1B3) ENSP00000261196.2:p.Pro114=
ENST00000381541.7:c.342A>T (SLCO1B3-SLCO1B7) ENSP00000370952.3:p.Pro114=
ENST00000381545.7:c.342A>T (SLCO1B3) ENSP00000370956.3:p.Pro114=
ENST00000540229.1:c.342A>T (SLCO1B3-SLCO1B7) ENSP00000441269.1:p.Pro114=
ENST00000540853.5:c.342A>T (SLCO1B3) ENSP00000442000.1:p.Pro114=
ENST00000545880.1:n.194A>T (SLCO1B3)
NM_019844.3:c.342A>T (SLCO1B3) NP_062818.1:p.Pro114=
NM_001349920.1:c.258A>T (SLCO1B3) NP_001336849.1:p.Pro86=
NM_001349920.2:c.258A>T (SLCO1B3) NP_001336849.1:p.Pro86=
NM_001371097.1:c.342A>T (SLCO1B3-SLCO1B7) NP_001358026.1:p.Pro114=
NM_019844.4:c.342A>T (SLCO1B3) MANE Select NP_062818.1:p.Pro114=