Canonical Allele Identifier: CA2020989718
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174830G= , CM000674.2:g.21174830G= GRCh38
NC_000012.11:g.21327764G= , CM000674.1:g.21327764G= GRCh37
NC_000012.10:g.21219031G= NCBI36
NG_011745.1:g.48637G= , LRG_1022:g.48637G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+121G= MANE Select ENSP00000256958.2:n.359+121G=
ENST00000256958.2:c.359+121G= ENSP00000256958.2:n.359+121G=
ENST00000543498.5:c.426-1946G=
NM_006446.4:c.359+121G= , LRG_1022t1:c.359+121G= NP_006437.3:n.359+121G=
NM_006446.5:c.359+121G= MANE Select NP_006437.3:n.359+121G=