Canonical Allele Identifier: CA603657595
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs952815153
gnomAD v2: 12-21327797-C-T
MyVariant Identifiers: chr12:g.21327797C>T (hg19) chr12:g.21174863C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174863C>T , CM000674.2:g.21174863C>T GRCh38
NC_000012.11:g.21327797C>T , CM000674.1:g.21327797C>T GRCh37
NC_000012.10:g.21219064C>T NCBI36
NG_011745.1:g.48670C>T , LRG_1022:g.48670C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+154C>T MANE Select ENSP00000256958.2:n.359+154C>T
ENST00000256958.2:c.359+154C>T ENSP00000256958.2:n.359+154C>T
ENST00000543498.5:c.426-1913C>T
NM_006446.4:c.359+154C>T , LRG_1022t1:c.359+154C>T NP_006437.3:n.359+154C>T
NM_006446.5:c.359+154C>T MANE Select NP_006437.3:n.359+154C>T
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