Canonical Allele Identifier: CA478863884
Gene: SLCO1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21349923T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21196989T>G , CM000674.2:g.21196989T>G GRCh38
NC_000012.11:g.21349923T>G , CM000674.1:g.21349923T>G GRCh37
NC_000012.10:g.21241190T>G NCBI36
NG_011745.1:g.70796T>G , LRG_1022:g.70796T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.771T>G MANE Select ENSP00000256958.2:p.Ala257=
ENST00000256958.2:c.771T>G ENSP00000256958.2:p.Ala257=
NM_006446.4:c.771T>G , LRG_1022t1:c.771T>G NP_006437.3:p.Ala257=
NM_006446.5:c.771T>G MANE Select NP_006437.3:p.Ala257=
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Search 100 bp 3'