Canonical Allele Identifier: CA2020975143

Gene: SLCO1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21138535T= , CM000674.2:g.21138535T=	GRCh38
NC_000012.11:g.21291469T= , CM000674.1:g.21291469T=	GRCh37
NC_000012.10:g.21182736T=	NCBI36
NG_011745.1:g.12342T= , LRG_1022:g.12342T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256958.3:c.-61-2979T= MANE Select	ENSP00000256958.2:n.-61-2979T=
ENST00000256958.2:c.-61-2979T=	ENSP00000256958.2:n.-61-2979T=
ENST00000543498.5:c.281-2979T=
ENST00000585342.5:c.485-2979T=	ENSP00000467594.1:n.485-2979T=
ENST00000590779.5:c.491-2979T=
ENST00000592513.1:c.472-2979T=
NM_006446.4:c.-61-2979T= , LRG_1022t1:c.-61-2979T=	NP_006437.3:n.-61-2979T=
NM_006446.5:c.-61-2979T= MANE Select	NP_006437.3:n.-61-2979T=