Canonical Allele Identifier: CA2020989635
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174649G= , CM000674.2:g.21174649G= GRCh38
NC_000012.11:g.21327583G= , CM000674.1:g.21327583G= GRCh37
NC_000012.10:g.21218850G= NCBI36
NG_011745.1:g.48456G= , LRG_1022:g.48456G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.299G= MANE Select ENSP00000256958.2:p.Gly100=
ENST00000256958.2:c.299G= ENSP00000256958.2:p.Gly100=
ENST00000543498.5:c.426-2127G=
NM_006446.4:c.299G= , LRG_1022t1:c.299G= NP_006437.3:p.Gly100=
NM_006446.5:c.299G= MANE Select NP_006437.3:p.Gly100=