Canonical Allele Identifier: CA2021009602
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215807C= , CM000674.2:g.21215807C= GRCh38
NC_000012.11:g.21368741C= , CM000674.1:g.21368741C= GRCh37
NC_000012.10:g.21260008C= NCBI36
NG_011745.1:g.89614C= , LRG_1022:g.89614C=

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.1498-1312C= MANE Select ENSP00000256958.2:n.1498-1312C=
ENST00000256958.2:c.1498-1312C= ENSP00000256958.2:n.1498-1312C=
NM_006446.4:c.1498-1312C= , LRG_1022t1:c.1498-1312C= NP_006437.3:n.1498-1312C=
NM_006446.5:c.1498-1312C= MANE Select NP_006437.3:n.1498-1312C=