Canonical Allele Identifier: CA233559974
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1053632845
gnomAD v3: 12-21174907-C-T
gnomAD v4: 12-21174907-C-T
MyVariant Identifiers: chr12:g.21327841C>T (hg19) chr12:g.21174907C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174907C>T , CM000674.2:g.21174907C>T GRCh38
NC_000012.11:g.21327841C>T , CM000674.1:g.21327841C>T GRCh37
NC_000012.10:g.21219108C>T NCBI36
NG_011745.1:g.48714C>T , LRG_1022:g.48714C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+198C>T MANE Select ENSP00000256958.2:n.359+198C>T
ENST00000256958.2:c.359+198C>T ENSP00000256958.2:n.359+198C>T
ENST00000543498.5:c.426-1869C>T
NM_006446.4:c.359+198C>T , LRG_1022t1:c.359+198C>T NP_006437.3:n.359+198C>T
NM_006446.5:c.359+198C>T MANE Select NP_006437.3:n.359+198C>T
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