Canonical Allele Identifier: CA478864337
Gene: SLCO1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21353578G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200644G>A , CM000674.2:g.21200644G>A GRCh38
NC_000012.11:g.21353578G>A , CM000674.1:g.21353578G>A GRCh37
NC_000012.10:g.21244845G>A NCBI36
NG_011745.1:g.74451G>A , LRG_1022:g.74451G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1107G>A MANE Select ENSP00000256958.2:p.Gln369=
ENST00000256958.2:c.1107G>A ENSP00000256958.2:p.Gln369=
NM_006446.4:c.1107G>A , LRG_1022t1:c.1107G>A NP_006437.3:p.Gln369=
NM_006446.5:c.1107G>A MANE Select NP_006437.3:p.Gln369=
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Search 100 bp 3'