Canonical Allele Identifier: CA2020989776
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174959T= , CM000674.2:g.21174959T= GRCh38
NC_000012.11:g.21327893T= , CM000674.1:g.21327893T= GRCh37
NC_000012.10:g.21219160T= NCBI36
NG_011745.1:g.48766T= , LRG_1022:g.48766T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+250T= MANE Select ENSP00000256958.2:n.359+250T=
ENST00000256958.2:c.359+250T= ENSP00000256958.2:n.359+250T=
ENST00000543498.5:c.426-1817T=
NM_006446.4:c.359+250T= , LRG_1022t1:c.359+250T= NP_006437.3:n.359+250T=
NM_006446.5:c.359+250T= MANE Select NP_006437.3:n.359+250T=