Canonical Allele Identifier: CA2020991438
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178603T= , CM000674.2:g.21178603T= GRCh38
NC_000012.11:g.21331537T= , CM000674.1:g.21331537T= GRCh37
NC_000012.10:g.21222804T= NCBI36
NG_011745.1:g.52410T= , LRG_1022:g.52410T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.509T= MANE Select ENSP00000256958.2:p.Met170=
ENST00000256958.2:c.509T= ENSP00000256958.2:p.Met170=
NM_006446.4:c.509T= , LRG_1022t1:c.509T= NP_006437.3:p.Met170=
NM_006446.5:c.509T= MANE Select NP_006437.3:p.Met170=