Canonical Allele Identifier: CA384092078
Gene: SLCO1B3 HGNC NCBI
SLCO1B3-SLCO1B7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20862764A>G , CM000674.2:g.20862764A>G GRCh38
NC_000012.11:g.21015698A>G , CM000674.1:g.21015698A>G GRCh37
NC_000012.10:g.20906965A>G NCBI36
NG_032071.1:g.57061A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381545.8:c.637A>G (SLCO1B3) MANE Select ENSP00000370956.4:p.Asn213Asp
ENST00000261196.6:c.637A>G (SLCO1B3) ENSP00000261196.2:p.Asn213Asp
ENST00000381541.7:c.359+4193A>G (SLCO1B3-SLCO1B7) ENSP00000370952.3:n.359+4193A>G
ENST00000381545.7:c.637A>G (SLCO1B3) ENSP00000370956.3:p.Asn213Asp
ENST00000540229.1:c.637A>G (SLCO1B3-SLCO1B7) ENSP00000441269.1:p.Asn213Asp
ENST00000540853.5:c.637A>G (SLCO1B3) ENSP00000442000.1:p.Asn213Asp
ENST00000544370.1:c.109A>G (SLCO1B3) ENSP00000443225.1:p.Asn37Asp
NM_019844.3:c.637A>G (SLCO1B3) NP_062818.1:p.Asn213Asp
NM_001349920.1:c.553A>G (SLCO1B3) NP_001336849.1:p.Asn185Asp
NM_001349920.2:c.553A>G (SLCO1B3) NP_001336849.1:p.Asn185Asp
NM_001371097.1:c.637A>G (SLCO1B3-SLCO1B7) NP_001358026.1:p.Asn213Asp
NM_019844.4:c.637A>G (SLCO1B3) MANE Select NP_062818.1:p.Asn213Asp