Canonical Allele Identifier: CA384106699
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1941146079
gnomAD v3: 12-21200609-T-C
gnomAD v4: 12-21200609-T-C
MyVariant Identifiers: chr12:g.21353543T>C (hg19) chr12:g.21200609T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200609T>C , CM000674.2:g.21200609T>C GRCh38
NC_000012.11:g.21353543T>C , CM000674.1:g.21353543T>C GRCh37
NC_000012.10:g.21244810T>C NCBI36
NG_011745.1:g.74416T>C , LRG_1022:g.74416T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.1072T>C MANE Select ENSP00000256958.2:p.Tyr358His
ENST00000256958.2:c.1072T>C ENSP00000256958.2:p.Tyr358His
NM_006446.4:c.1072T>C , LRG_1022t1:c.1072T>C NP_006437.3:p.Tyr358His
NM_006446.5:c.1072T>C MANE Select NP_006437.3:p.Tyr358His
Search 100 bp 5'
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