Canonical Allele Identifier: CA478866822

Gene: SLCO1B1

Linked Data

• MyVariant Identifiers: chr12:g.21329770C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21176836C>G , CM000674.2:g.21176836C>G	GRCh38
NC_000012.11:g.21329770C>G , CM000674.1:g.21329770C>G	GRCh37
NC_000012.10:g.21221037C>G	NCBI36
NG_011745.1:g.50643C>G , LRG_1022:g.50643C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256958.3:c.420C>G MANE Select	ENSP00000256958.2:p.Ser140=
ENST00000256958.2:c.420C>G	ENSP00000256958.2:p.Ser140=
ENST00000543498.5:c.486C>G
NM_006446.4:c.420C>G , LRG_1022t1:c.420C>G	NP_006437.3:p.Ser140=
NM_006446.5:c.420C>G MANE Select	NP_006437.3:p.Ser140=