Canonical Allele Identifier: CA2020991397
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178525T= , CM000674.2:g.21178525T= GRCh38
NC_000012.11:g.21331459T= , CM000674.1:g.21331459T= GRCh37
NC_000012.10:g.21222726T= NCBI36
NG_011745.1:g.52332T= , LRG_1022:g.52332T=

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.482-51T= MANE Select ENSP00000256958.2:n.482-51T=
ENST00000256958.2:c.482-51T= ENSP00000256958.2:n.482-51T=
NM_006446.4:c.482-51T= , LRG_1022t1:c.482-51T= NP_006437.3:n.482-51T=
NM_006446.5:c.482-51T= MANE Select NP_006437.3:n.482-51T=