Canonical Allele Identifier: CA2021001380
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1941143825

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200498A>T , CM000674.2:g.21200498A>T GRCh38
NC_000012.11:g.21353432A>T , CM000674.1:g.21353432A>T GRCh37
NC_000012.10:g.21244699A>T NCBI36
NG_011745.1:g.74305A>T , LRG_1022:g.74305A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.971-10A>T MANE Select ENSP00000256958.2:n.971-10A>T
ENST00000256958.2:c.971-10A>T ENSP00000256958.2:n.971-10A>T
NM_006446.4:c.971-10A>T , LRG_1022t1:c.971-10A>T NP_006437.3:n.971-10A>T
NM_006446.5:c.971-10A>T MANE Select NP_006437.3:n.971-10A>T