Canonical Allele Identifier: CA6476720
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs141467543
ExAC: 12:21331546 A / G
gnomAD v2: 12-21331546-A-G
gnomAD v3: 12-21178612-A-G
gnomAD v4: 12-21178612-A-G
MyVariant Identifiers: chr12:g.21331546A>G (hg19) chr12:g.21178612A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178612A>G , CM000674.2:g.21178612A>G GRCh38
NC_000012.11:g.21331546A>G , CM000674.1:g.21331546A>G GRCh37
NC_000012.10:g.21222813A>G NCBI36
NG_011745.1:g.52419A>G , LRG_1022:g.52419A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.518A>G MANE Select ENSP00000256958.2:p.Tyr173Cys
ENST00000256958.2:c.518A>G ENSP00000256958.2:p.Tyr173Cys
NM_006446.4:c.518A>G , LRG_1022t1:c.518A>G NP_006437.3:p.Tyr173Cys
NM_006446.5:c.518A>G MANE Select NP_006437.3:p.Tyr173Cys
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