Canonical Allele Identifier: CA478866959
Gene: SLCO1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21329830A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176896A>G , CM000674.2:g.21176896A>G GRCh38
NC_000012.11:g.21329830A>G , CM000674.1:g.21329830A>G GRCh37
NC_000012.10:g.21221097A>G NCBI36
NG_011745.1:g.50703A>G , LRG_1022:g.50703A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.480A>G MANE Select ENSP00000256958.2:p.Lys160=
ENST00000256958.2:c.480A>G ENSP00000256958.2:p.Lys160=
NM_006446.4:c.480A>G , LRG_1022t1:c.480A>G NP_006437.3:p.Lys160=
NM_006446.5:c.480A>G MANE Select NP_006437.3:p.Lys160=