Canonical Allele Identifier: CA2020989790
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174988T= , CM000674.2:g.21174988T= GRCh38
NC_000012.11:g.21327922T= , CM000674.1:g.21327922T= GRCh37
NC_000012.10:g.21219189T= NCBI36
NG_011745.1:g.48795T= , LRG_1022:g.48795T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+279T= MANE Select ENSP00000256958.2:n.359+279T=
ENST00000256958.2:c.359+279T= ENSP00000256958.2:n.359+279T=
ENST00000543498.5:c.426-1788T=
NM_006446.4:c.359+279T= , LRG_1022t1:c.359+279T= NP_006437.3:n.359+279T=
NM_006446.5:c.359+279T= MANE Select NP_006437.3:n.359+279T=