Canonical Allele Identifier: CA2020999836
Gene: SLCO1B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21196907A= , CM000674.2:g.21196907A= GRCh38
NC_000012.11:g.21349841A= , CM000674.1:g.21349841A= GRCh37
NC_000012.10:g.21241108A= NCBI36
NG_011745.1:g.70714A= , LRG_1022:g.70714A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.728-39A= MANE Select ENSP00000256958.2:n.728-39A=
ENST00000256958.2:c.728-39A= ENSP00000256958.2:n.728-39A=
NM_006446.4:c.728-39A= , LRG_1022t1:c.728-39A= NP_006437.3:n.728-39A=
NM_006446.5:c.728-39A= MANE Select NP_006437.3:n.728-39A=
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