Canonical Allele Identifier: CA478866490

Gene: SLCO1B1

Linked Data

• MyVariant Identifiers: chr12:g.21327555C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21174621C>T , CM000674.2:g.21174621C>T	GRCh38
NC_000012.11:g.21327555C>T , CM000674.1:g.21327555C>T	GRCh37
NC_000012.10:g.21218822C>T	NCBI36
NG_011745.1:g.48428C>T , LRG_1022:g.48428C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000256958.3:c.271C>T MANE Select	ENSP00000256958.2:p.Leu91=
ENST00000256958.2:c.271C>T	ENSP00000256958.2:p.Leu91=
ENST00000543498.5:c.426-2155C>T
NM_006446.4:c.271C>T , LRG_1022t1:c.271C>T	NP_006437.3:p.Leu91=
NM_006446.5:c.271C>T MANE Select	NP_006437.3:p.Leu91=