Canonical Allele Identifier: CA384104056
Gene: SLCO1B1 HGNC NCBI

Linked Data

gnomAD v4: 12-21174577-G-C
MyVariant Identifiers: chr12:g.21327511G>C (hg19) chr12:g.21174577G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174577G>C , CM000674.2:g.21174577G>C GRCh38
NC_000012.11:g.21327511G>C , CM000674.1:g.21327511G>C GRCh37
NC_000012.10:g.21218778G>C NCBI36
NG_011745.1:g.48384G>C , LRG_1022:g.48384G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.227G>C MANE Select ENSP00000256958.2:p.Gly76Ala
ENST00000256958.2:c.227G>C ENSP00000256958.2:p.Gly76Ala
ENST00000543498.5:c.426-2199G>C
NM_006446.4:c.227G>C , LRG_1022t1:c.227G>C NP_006437.3:p.Gly76Ala
NM_006446.5:c.227G>C MANE Select NP_006437.3:p.Gly76Ala
Search 100 bp 5'
Search 100 bp 3'