Canonical Allele Identifier: CA233562316
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1049096483
MyVariant Identifiers: chr12:g.21331572G>T (hg19) chr12:g.21178638G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178638G>T , CM000674.2:g.21178638G>T GRCh38
NC_000012.11:g.21331572G>T , CM000674.1:g.21331572G>T GRCh37
NC_000012.10:g.21222839G>T NCBI36
NG_011745.1:g.52445G>T , LRG_1022:g.52445G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.544G>T MANE Select ENSP00000256958.2:p.Gly182Ter
ENST00000256958.2:c.544G>T ENSP00000256958.2:p.Gly182Ter
NM_006446.4:c.544G>T , LRG_1022t1:c.544G>T NP_006437.3:p.Gly182Ter
NM_006446.5:c.544G>T MANE Select NP_006437.3:p.Gly182Ter
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Search 100 bp 3'