Canonical Allele Identifier: CA2021001388
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200514T= , CM000674.2:g.21200514T= GRCh38
NC_000012.11:g.21353448T= , CM000674.1:g.21353448T= GRCh37
NC_000012.10:g.21244715T= NCBI36
NG_011745.1:g.74321T= , LRG_1022:g.74321T=

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.977T= MANE Select ENSP00000256958.2:p.Phe326=
ENST00000256958.2:c.977T= ENSP00000256958.2:p.Phe326=
NM_006446.4:c.977T= , LRG_1022t1:c.977T= NP_006437.3:p.Phe326=
NM_006446.5:c.977T= MANE Select NP_006437.3:p.Phe326=