Canonical Allele Identifier: CA2020989781
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174971C= , CM000674.2:g.21174971C= GRCh38
NC_000012.11:g.21327905C= , CM000674.1:g.21327905C= GRCh37
NC_000012.10:g.21219172C= NCBI36
NG_011745.1:g.48778C= , LRG_1022:g.48778C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+262C= MANE Select ENSP00000256958.2:n.359+262C=
ENST00000256958.2:c.359+262C= ENSP00000256958.2:n.359+262C=
ENST00000543498.5:c.426-1805C=
NM_006446.4:c.359+262C= , LRG_1022t1:c.359+262C= NP_006437.3:n.359+262C=
NM_006446.5:c.359+262C= MANE Select NP_006437.3:n.359+262C=