Canonical Allele Identifier: CA384104430
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1394287543

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174708T>A , CM000674.2:g.21174708T>A GRCh38
NC_000012.11:g.21327642T>A , CM000674.1:g.21327642T>A GRCh37
NC_000012.10:g.21218909T>A NCBI36
NG_011745.1:g.48515T>A , LRG_1022:g.48515T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.358T>A MANE Select ENSP00000256958.2:p.Tyr120Asn
ENST00000256958.2:c.358T>A ENSP00000256958.2:p.Tyr120Asn
ENST00000543498.5:c.426-2068T>A
NM_006446.4:c.358T>A , LRG_1022t1:c.358T>A NP_006437.3:p.Tyr120Asn
NM_006446.5:c.358T>A MANE Select NP_006437.3:p.Tyr120Asn