Canonical Allele Identifier: CA6476721
Gene: SLCO1B1 HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.518A>C MANE Select ENSP00000256958.2:p.Tyr173Ser
ENST00000256958.2:c.518A>C ENSP00000256958.2:p.Tyr173Ser
NM_006446.4:c.518A>C , LRG_1022t1:c.518A>C NP_006437.3:p.Tyr173Ser
NM_006446.5:c.518A>C MANE Select NP_006437.3:p.Tyr173Ser
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