Canonical Allele Identifier: CA2020999885
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21196992G= , CM000674.2:g.21196992G= GRCh38
NC_000012.11:g.21349926G= , CM000674.1:g.21349926G= GRCh37
NC_000012.10:g.21241193G= NCBI36
NG_011745.1:g.70799G= , LRG_1022:g.70799G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.774G= MANE Select ENSP00000256958.2:p.Trp258=
ENST00000256958.2:c.774G= ENSP00000256958.2:p.Trp258=
NM_006446.4:c.774G= , LRG_1022t1:c.774G= NP_006437.3:p.Trp258=
NM_006446.5:c.774G= MANE Select NP_006437.3:p.Trp258=