Canonical Allele Identifier: CA384105537
Gene: SLCO1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21331565G>C (hg19) chr12:g.21178631G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178631G>C , CM000674.2:g.21178631G>C GRCh38
NC_000012.11:g.21331565G>C , CM000674.1:g.21331565G>C GRCh37
NC_000012.10:g.21222832G>C NCBI36
NG_011745.1:g.52438G>C , LRG_1022:g.52438G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.537G>C MANE Select ENSP00000256958.2:p.Met179Ile
ENST00000256958.2:c.537G>C ENSP00000256958.2:p.Met179Ile
NM_006446.4:c.537G>C , LRG_1022t1:c.537G>C NP_006437.3:p.Met179Ile
NM_006446.5:c.537G>C MANE Select NP_006437.3:p.Met179Ile
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