Canonical Allele Identifier: CA384104059
Gene: SLCO1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21327513A>G (hg19) chr12:g.21174579A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174579A>G , CM000674.2:g.21174579A>G GRCh38
NC_000012.11:g.21327513A>G , CM000674.1:g.21327513A>G GRCh37
NC_000012.10:g.21218780A>G NCBI36
NG_011745.1:g.48386A>G , LRG_1022:g.48386A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.229A>G MANE Select ENSP00000256958.2:p.Asn77Asp
ENST00000256958.2:c.229A>G ENSP00000256958.2:p.Asn77Asp
ENST00000543498.5:c.426-2197A>G
NM_006446.4:c.229A>G , LRG_1022t1:c.229A>G NP_006437.3:p.Asn77Asp
NM_006446.5:c.229A>G MANE Select NP_006437.3:p.Asn77Asp
Search 100 bp 5'
Search 100 bp 3'