Canonical Allele Identifier: CA384104809
Gene: SLCO1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21329742C>G (hg19) chr12:g.21176808C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176808C>G , CM000674.2:g.21176808C>G GRCh38
NC_000012.11:g.21329742C>G , CM000674.1:g.21329742C>G GRCh37
NC_000012.10:g.21221009C>G NCBI36
NG_011745.1:g.50615C>G , LRG_1022:g.50615C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.392C>G MANE Select ENSP00000256958.2:p.Ser131Ter
ENST00000256958.2:c.392C>G ENSP00000256958.2:p.Ser131Ter
ENST00000543498.5:c.458C>G
NM_006446.4:c.392C>G , LRG_1022t1:c.392C>G NP_006437.3:p.Ser131Ter
NM_006446.5:c.392C>G MANE Select NP_006437.3:p.Ser131Ter
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