Canonical Allele Identifier: CA233560043

Gene: SLCO1B1

Linked Data

• dbSNP Id: rs987050130
• MyVariant Identifiers: chr12:g.21328001C>T (hg19) ; chr12:g.21175067C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21175067C>T , CM000674.2:g.21175067C>T	GRCh38
NC_000012.11:g.21328001C>T , CM000674.1:g.21328001C>T	GRCh37
NC_000012.10:g.21219268C>T	NCBI36
NG_011745.1:g.48874C>T , LRG_1022:g.48874C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256958.3:c.359+358C>T MANE Select	ENSP00000256958.2:n.359+358C>T
ENST00000256958.2:c.359+358C>T	ENSP00000256958.2:n.359+358C>T
ENST00000543498.5:c.426-1709C>T
NM_006446.4:c.359+358C>T , LRG_1022t1:c.359+358C>T	NP_006437.3:n.359+358C>T
NM_006446.5:c.359+358C>T MANE Select	NP_006437.3:n.359+358C>T