Canonical Allele Identifier: CA6476749
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs750338584
ExAC: 12:21331639 A / G
gnomAD v2: 12-21331639-A-G
gnomAD v3: 12-21178705-A-G
gnomAD v4: 12-21178705-A-G
MyVariant Identifiers: chr12:g.21331639A>G (hg19) chr12:g.21178705A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178705A>G , CM000674.2:g.21178705A>G GRCh38
NC_000012.11:g.21331639A>G , CM000674.1:g.21331639A>G GRCh37
NC_000012.10:g.21222906A>G NCBI36
NG_011745.1:g.52512A>G , LRG_1022:g.52512A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.611A>G MANE Select ENSP00000256958.2:p.His204Arg
ENST00000256958.2:c.611A>G ENSP00000256958.2:p.His204Arg
NM_006446.4:c.611A>G , LRG_1022t1:c.611A>G NP_006437.3:p.His204Arg
NM_006446.5:c.611A>G MANE Select NP_006437.3:p.His204Arg
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