Canonical Allele Identifier: CA6477018
Gene: SLCO1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 307954
ClinVar RCV Id: RCV000355032
dbSNP Id: rs59502379
ExAC: 12:21358933 G / C
gnomAD v2: 12-21358933-G-C
gnomAD v3: 12-21205999-G-C
gnomAD v4: 12-21205999-G-C
MyVariant Identifiers: chr12:g.21358933G>C (hg19) chr12:g.21205999G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21205999G>C , CM000674.2:g.21205999G>C GRCh38
NC_000012.11:g.21358933G>C , CM000674.1:g.21358933G>C GRCh37
NC_000012.10:g.21250200G>C NCBI36
NG_011745.1:g.79806G>C , LRG_1022:g.79806G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1463G>C MANE Select ENSP00000256958.2:p.Gly488Ala
ENST00000256958.2:c.1463G>C ENSP00000256958.2:p.Gly488Ala
NM_006446.4:c.1463G>C , LRG_1022t1:c.1463G>C NP_006437.3:p.Gly488Ala
NM_006446.5:c.1463G>C MANE Select NP_006437.3:p.Gly488Ala
Search 100 bp 5'
Search 100 bp 3'