Canonical Allele Identifier: CA13581915
Gene: SLCO1B3 HGNC NCBI
SLCO1B3-SLCO1B7 HGNC NCBI

Linked Data

dbSNP Id: rs11045585

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20892760A>G , CM000674.2:g.20892760A>G GRCh38
NC_000012.11:g.21045694A>G , CM000674.1:g.21045694A>G GRCh37
NC_000012.10:g.20936961A>G NCBI36
NG_032071.1:g.87057A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000381545.8:c.1683-5676A>G (SLCO1B3) MANE Select ENSP00000370956.4:n.1683-5676A>G
ENST00000261196.6:c.1683-5676A>G (SLCO1B3) ENSP00000261196.2:n.1683-5676A>G
ENST00000381541.7:c.359+34189A>G (SLCO1B3-SLCO1B7) ENSP00000370952.3:n.359+34189A>G
ENST00000381545.7:c.1683-5676A>G (SLCO1B3) ENSP00000370956.3:n.1683-5676A>G
ENST00000540229.1:c.1683-5676A>G (SLCO1B3-SLCO1B7) ENSP00000441269.1:n.1683-5676A>G
ENST00000544370.1:c.1155-5676A>G (SLCO1B3) ENSP00000443225.1:n.1155-5676A>G
NM_019844.3:c.1683-5676A>G (SLCO1B3) NP_062818.1:n.1683-5676A>G
NM_001349920.1:c.1599-5676A>G (SLCO1B3) NP_001336849.1:n.1599-5676A>G
NM_001349920.2:c.1599-5676A>G (SLCO1B3) NP_001336849.1:n.1599-5676A>G
NM_001371097.1:c.1683-5676A>G (SLCO1B3-SLCO1B7) NP_001358026.1:n.1683-5676A>G
NM_019844.4:c.1683-5676A>G (SLCO1B3) MANE Select NP_062818.1:n.1683-5676A>G