Canonical Allele Identifier: CA233552798
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1871395

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21199381A>G , CM000674.2:g.21199381A>G GRCh38
NC_000012.11:g.21352315A>G , CM000674.1:g.21352315A>G GRCh37
NC_000012.10:g.21243582A>G NCBI36
NG_011745.1:g.73188A>G , LRG_1022:g.73188A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.971-1127A>G MANE Select ENSP00000256958.2:n.971-1127A>G
ENST00000256958.2:c.971-1127A>G ENSP00000256958.2:n.971-1127A>G
NM_006446.4:c.971-1127A>G , LRG_1022t1:c.971-1127A>G NP_006437.3:n.971-1127A>G
NM_006446.5:c.971-1127A>G MANE Select NP_006437.3:n.971-1127A>G