Canonical Allele Identifier: CA233562172
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1011764892
gnomAD v2: 12-21331493-C-T
gnomAD v3: 12-21178559-C-T
gnomAD v4: 12-21178559-C-T
MyVariant Identifiers: chr12:g.21331493C>T (hg19) chr12:g.21178559C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178559C>T , CM000674.2:g.21178559C>T GRCh38
NC_000012.11:g.21331493C>T , CM000674.1:g.21331493C>T GRCh37
NC_000012.10:g.21222760C>T NCBI36
NG_011745.1:g.52366C>T , LRG_1022:g.52366C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.482-17C>T MANE Select ENSP00000256958.2:n.482-17C>T
ENST00000256958.2:c.482-17C>T ENSP00000256958.2:n.482-17C>T
NM_006446.4:c.482-17C>T , LRG_1022t1:c.482-17C>T NP_006437.3:n.482-17C>T
NM_006446.5:c.482-17C>T MANE Select NP_006437.3:n.482-17C>T
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