Canonical Allele Identifier: CA2020991449
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178621_21178622delinsTG , CM000674.2:g.21178621_21178622delinsTG GRCh38
NC_000012.11:g.21331555_21331556delinsTG , CM000674.1:g.21331555_21331556delinsTG GRCh37
NC_000012.10:g.21222822_21222823delinsTG NCBI36
NG_011745.1:g.52428_52429delinsTG , LRG_1022:g.52428_52429delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.527_528delinsTG MANE Select ENSP00000256958.2:p.Met176=
ENST00000256958.2:c.527_528delinsTG ENSP00000256958.2:p.Met176=
NM_006446.4:c.527_528delinsTG , LRG_1022t1:c.527_528delinsTG NP_006437.3:p.Met176=
NM_006446.5:c.527_528delinsTG MANE Select NP_006437.3:p.Met176=