Canonical Allele Identifier: CA478866739
Gene: SLCO1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21329714A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176780A>C , CM000674.2:g.21176780A>C GRCh38
NC_000012.11:g.21329714A>C , CM000674.1:g.21329714A>C GRCh37
NC_000012.10:g.21220981A>C NCBI36
NG_011745.1:g.50587A>C , LRG_1022:g.50587A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.364A>C MANE Select ENSP00000256958.2:p.Arg122=
ENST00000256958.2:c.364A>C ENSP00000256958.2:p.Arg122=
ENST00000543498.5:c.430A>C
NM_006446.4:c.364A>C , LRG_1022t1:c.364A>C NP_006437.3:p.Arg122=
NM_006446.5:c.364A>C MANE Select NP_006437.3:p.Arg122=