Canonical Allele Identifier: CA384106702
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1482611365
gnomAD v2: 12-21353545-T-A
gnomAD v4: 12-21200611-T-A
MyVariant Identifiers: chr12:g.21353545T>A (hg19) chr12:g.21200611T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200611T>A , CM000674.2:g.21200611T>A GRCh38
NC_000012.11:g.21353545T>A , CM000674.1:g.21353545T>A GRCh37
NC_000012.10:g.21244812T>A NCBI36
NG_011745.1:g.74418T>A , LRG_1022:g.74418T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1074T>A MANE Select ENSP00000256958.2:p.Tyr358Ter
ENST00000256958.2:c.1074T>A ENSP00000256958.2:p.Tyr358Ter
NM_006446.4:c.1074T>A , LRG_1022t1:c.1074T>A NP_006437.3:p.Tyr358Ter
NM_006446.5:c.1074T>A MANE Select NP_006437.3:p.Tyr358Ter
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