Canonical Allele Identifier: CA2021009540
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1941349338

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215693T>C , CM000674.2:g.21215693T>C GRCh38
NC_000012.11:g.21368627T>C , CM000674.1:g.21368627T>C GRCh37
NC_000012.10:g.21259894T>C NCBI36
NG_011745.1:g.89500T>C , LRG_1022:g.89500T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.1498-1426T>C MANE Select ENSP00000256958.2:n.1498-1426T>C
ENST00000256958.2:c.1498-1426T>C ENSP00000256958.2:n.1498-1426T>C
NM_006446.4:c.1498-1426T>C , LRG_1022t1:c.1498-1426T>C NP_006437.3:n.1498-1426T>C
NM_006446.5:c.1498-1426T>C MANE Select NP_006437.3:n.1498-1426T>C