Canonical Allele Identifier: CA384106729
Gene: SLCO1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21353556A>G (hg19) chr12:g.21200622A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200622A>G , CM000674.2:g.21200622A>G GRCh38
NC_000012.11:g.21353556A>G , CM000674.1:g.21353556A>G GRCh37
NC_000012.10:g.21244823A>G NCBI36
NG_011745.1:g.74429A>G , LRG_1022:g.74429A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1085A>G MANE Select ENSP00000256958.2:p.Tyr362Cys
ENST00000256958.2:c.1085A>G ENSP00000256958.2:p.Tyr362Cys
NM_006446.4:c.1085A>G , LRG_1022t1:c.1085A>G NP_006437.3:p.Tyr362Cys
NM_006446.5:c.1085A>G MANE Select NP_006437.3:p.Tyr362Cys
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