Canonical Allele Identifier: CA384106767

Gene: SLCO1B1

Linked Data

• MyVariant Identifiers: chr12:g.21353573G>T (hg19) ; chr12:g.21200639G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21200639G>T , CM000674.2:g.21200639G>T	GRCh38
NC_000012.11:g.21353573G>T , CM000674.1:g.21353573G>T	GRCh37
NC_000012.10:g.21244840G>T	NCBI36
NG_011745.1:g.74446G>T , LRG_1022:g.74446G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256958.3:c.1102G>T MANE Select	ENSP00000256958.2:p.Gly368Cys
ENST00000256958.2:c.1102G>T	ENSP00000256958.2:p.Gly368Cys
NM_006446.4:c.1102G>T , LRG_1022t1:c.1102G>T	NP_006437.3:p.Gly368Cys
NM_006446.5:c.1102G>T MANE Select	NP_006437.3:p.Gly368Cys