Canonical Allele Identifier: CA233539103
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs909642995
MyVariant Identifiers: chr12:g.21291520T>G (hg19) chr12:g.21138586T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21138586T>G , CM000674.2:g.21138586T>G GRCh38
NC_000012.11:g.21291520T>G , CM000674.1:g.21291520T>G GRCh37
NC_000012.10:g.21182787T>G NCBI36
NG_011745.1:g.12393T>G , LRG_1022:g.12393T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.-61-2928T>G MANE Select ENSP00000256958.2:n.-61-2928T>G
ENST00000256958.2:c.-61-2928T>G ENSP00000256958.2:n.-61-2928T>G
ENST00000543498.5:c.281-2928T>G
ENST00000585342.5:c.485-2928T>G ENSP00000467594.1:n.485-2928T>G
ENST00000590779.5:c.491-2928T>G
ENST00000592513.1:c.472-2928T>G
NM_006446.4:c.-61-2928T>G , LRG_1022t1:c.-61-2928T>G NP_006437.3:n.-61-2928T>G
NM_006446.5:c.-61-2928T>G MANE Select NP_006437.3:n.-61-2928T>G
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