Canonical Allele Identifier: CA2020975151
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1940260942

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21138539A>T , CM000674.2:g.21138539A>T GRCh38
NC_000012.11:g.21291473A>T , CM000674.1:g.21291473A>T GRCh37
NC_000012.10:g.21182740A>T NCBI36
NG_011745.1:g.12346A>T , LRG_1022:g.12346A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.-61-2975A>T MANE Select ENSP00000256958.2:n.-61-2975A>T
ENST00000256958.2:c.-61-2975A>T ENSP00000256958.2:n.-61-2975A>T
ENST00000543498.5:c.281-2975A>T
ENST00000585342.5:c.485-2975A>T ENSP00000467594.1:n.485-2975A>T
ENST00000590779.5:c.491-2975A>T
ENST00000592513.1:c.472-2975A>T
NM_006446.4:c.-61-2975A>T , LRG_1022t1:c.-61-2975A>T NP_006437.3:n.-61-2975A>T
NM_006446.5:c.-61-2975A>T MANE Select NP_006437.3:n.-61-2975A>T