Canonical Allele Identifier: CA2020990590
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176782G= , CM000674.2:g.21176782G= GRCh38
NC_000012.11:g.21329716G= , CM000674.1:g.21329716G= GRCh37
NC_000012.10:g.21220983G= NCBI36
NG_011745.1:g.50589G= , LRG_1022:g.50589G=

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.366G= MANE Select ENSP00000256958.2:p.Arg122=
ENST00000256958.2:c.366G= ENSP00000256958.2:p.Arg122=
ENST00000543498.5:c.432G=
NM_006446.4:c.366G= , LRG_1022t1:c.366G= NP_006437.3:p.Arg122=
NM_006446.5:c.366G= MANE Select NP_006437.3:p.Arg122=