Canonical Allele Identifier: CA2021009508
Gene: SLCO1B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215622C= , CM000674.2:g.21215622C= GRCh38
NC_000012.11:g.21368556C= , CM000674.1:g.21368556C= GRCh37
NC_000012.10:g.21259823C= NCBI36
NG_011745.1:g.89429C= , LRG_1022:g.89429C=

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.1498-1497C= MANE Select ENSP00000256958.2:n.1498-1497C=
ENST00000256958.2:c.1498-1497C= ENSP00000256958.2:n.1498-1497C=
NM_006446.4:c.1498-1497C= , LRG_1022t1:c.1498-1497C= NP_006437.3:n.1498-1497C=
NM_006446.5:c.1498-1497C= MANE Select NP_006437.3:n.1498-1497C=
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