Canonical Allele Identifier: CA2020990539
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176630C= , CM000674.2:g.21176630C= GRCh38
NC_000012.11:g.21329564C= , CM000674.1:g.21329564C= GRCh37
NC_000012.10:g.21220831C= NCBI36
NG_011745.1:g.50437C= , LRG_1022:g.50437C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.360-146C= MANE Select ENSP00000256958.2:n.360-146C=
ENST00000256958.2:c.360-146C= ENSP00000256958.2:n.360-146C=
ENST00000543498.5:c.426-146C=
NM_006446.4:c.360-146C= , LRG_1022t1:c.360-146C= NP_006437.3:n.360-146C=
NM_006446.5:c.360-146C= MANE Select NP_006437.3:n.360-146C=