Canonical Allele Identifier: CA2020989565
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174502A= , CM000674.2:g.21174502A= GRCh38
NC_000012.11:g.21327436A= , CM000674.1:g.21327436A= GRCh37
NC_000012.10:g.21218703A= NCBI36
NG_011745.1:g.48309A= , LRG_1022:g.48309A=

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.227-75A= MANE Select ENSP00000256958.2:n.227-75A=
ENST00000256958.2:c.227-75A= ENSP00000256958.2:n.227-75A=
ENST00000543498.5:c.426-2274A=
NM_006446.4:c.227-75A= , LRG_1022t1:c.227-75A= NP_006437.3:n.227-75A=
NM_006446.5:c.227-75A= MANE Select NP_006437.3:n.227-75A=