Canonical Allele Identifier: CA686380226
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1215065059
gnomAD v2: 12-21368463-A-C
gnomAD v3: 12-21215529-A-C
gnomAD v4: 12-21215529-A-C
MyVariant Identifiers: chr12:g.21368463A>C (hg19) chr12:g.21215529A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215529A>C , CM000674.2:g.21215529A>C GRCh38
NC_000012.11:g.21368463A>C , CM000674.1:g.21368463A>C GRCh37
NC_000012.10:g.21259730A>C NCBI36
NG_011745.1:g.89336A>C , LRG_1022:g.89336A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1498-1590A>C MANE Select ENSP00000256958.2:n.1498-1590A>C
ENST00000256958.2:c.1498-1590A>C ENSP00000256958.2:n.1498-1590A>C
NM_006446.4:c.1498-1590A>C , LRG_1022t1:c.1498-1590A>C NP_006437.3:n.1498-1590A>C
NM_006446.5:c.1498-1590A>C MANE Select NP_006437.3:n.1498-1590A>C
Search 100 bp 5'
Search 100 bp 3'