Canonical Allele Identifier: CA478866940
Gene: SLCO1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21329821A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176887A>T , CM000674.2:g.21176887A>T GRCh38
NC_000012.11:g.21329821A>T , CM000674.1:g.21329821A>T GRCh37
NC_000012.10:g.21221088A>T NCBI36
NG_011745.1:g.50694A>T , LRG_1022:g.50694A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.471A>T MANE Select ENSP00000256958.2:p.Ile157=
ENST00000256958.2:c.471A>T ENSP00000256958.2:p.Ile157=
ENST00000543498.5:c.537A>T
NM_006446.4:c.471A>T , LRG_1022t1:c.471A>T NP_006437.3:p.Ile157=
NM_006446.5:c.471A>T MANE Select NP_006437.3:p.Ile157=