Canonical Allele Identifier: CA478866333
Gene: SLCO1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21327512A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174578A>G , CM000674.2:g.21174578A>G GRCh38
NC_000012.11:g.21327512A>G , CM000674.1:g.21327512A>G GRCh37
NC_000012.10:g.21218779A>G NCBI36
NG_011745.1:g.48385A>G , LRG_1022:g.48385A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.228A>G MANE Select ENSP00000256958.2:p.Gly76=
ENST00000256958.2:c.228A>G ENSP00000256958.2:p.Gly76=
ENST00000543498.5:c.426-2198A>G
NM_006446.4:c.228A>G , LRG_1022t1:c.228A>G NP_006437.3:p.Gly76=
NM_006446.5:c.228A>G MANE Select NP_006437.3:p.Gly76=
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