Canonical Allele Identifier: CA2021001444
Gene: SLCO1B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200610A= , CM000674.2:g.21200610A= GRCh38
NC_000012.11:g.21353544A= , CM000674.1:g.21353544A= GRCh37
NC_000012.10:g.21244811A= NCBI36
NG_011745.1:g.74417A= , LRG_1022:g.74417A=

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.1073A= MANE Select ENSP00000256958.2:p.Tyr358=
ENST00000256958.2:c.1073A= ENSP00000256958.2:p.Tyr358=
NM_006446.4:c.1073A= , LRG_1022t1:c.1073A= NP_006437.3:p.Tyr358=
NM_006446.5:c.1073A= MANE Select NP_006437.3:p.Tyr358=
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