Canonical Allele Identifier: CA2020989819
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21175061_21175062delinsTC , CM000674.2:g.21175061_21175062delinsTC GRCh38
NC_000012.11:g.21327995_21327996delinsTC , CM000674.1:g.21327995_21327996delinsTC GRCh37
NC_000012.10:g.21219262_21219263delinsTC NCBI36
NG_011745.1:g.48868_48869delinsTC , LRG_1022:g.48868_48869delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+352_359+353delinsTC MANE Select ENSP00000256958.2:n.359+352_359+353delinsTC
ENST00000256958.2:c.359+352_359+353delinsTC ENSP00000256958.2:n.359+352_359+353delinsTC
ENST00000543498.5:c.426-1715_426-1714delinsTC
NM_006446.4:c.359+352_359+353delinsTC , LRG_1022t1:c.359+352_359+353delinsTC NP_006437.3:n.359+352_359+353delinsTC
NM_006446.5:c.359+352_359+353delinsTC MANE Select NP_006437.3:n.359+352_359+353delinsTC