Canonical Allele Identifier: CA233562028
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs761384002

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178457_21178460del , CM000674.2:g.21178457_21178460del GRCh38
NC_000012.11:g.21331391_21331394del , CM000674.1:g.21331391_21331394del GRCh37
NC_000012.10:g.21222658_21222661del NCBI36
NG_011745.1:g.52264_52267del , LRG_1022:g.52264_52267del

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.482-119_482-116del MANE Select ENSP00000256958.2:n.482-119_482-116del
ENST00000256958.2:c.482-119_482-116del ENSP00000256958.2:n.482-119_482-116del
NM_006446.4:c.482-119_482-116del , LRG_1022t1:c.482-119_482-116del NP_006437.3:n.482-119_482-116del
NM_006446.5:c.482-119_482-116del MANE Select NP_006437.3:n.482-119_482-116del