Canonical Allele Identifier: CA13762915
Gene: SLCO1B3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2417940

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20864941T>C , CM000674.2:g.20864941T>C GRCh38
NC_000012.11:g.21017875T>C , CM000674.1:g.21017875T>C GRCh37
NC_000012.10:g.20909142T>C NCBI36
NG_032071.1:g.59238T>C

Transcript Alleles

HGVS Amino-acid change
NM_019844.3:c.727+2087T>C VV NP_062818.1:p.=
NM_001349920.1:c.643+2087T>C VV NP_001336849.1:p.=
ENST00000261196.6:c.727+2087T>C ENSP00000261196.2:p.=
ENST00000381541.7:c.359+6370T>C ENSP00000370952.3:p.=
ENST00000381545.7:c.727+2087T>C ENSP00000370956.3:p.=
ENST00000540229.1:c.727+2087T>C ENSP00000441269.1:p.=
ENST00000540853.5:c.727+2087T>C ENSP00000442000.1:p.=
ENST00000544370.1:n.199+2087T>C ENSP00000443225.1:p.=