Canonical Allele Identifier: CA6476728
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs371375183
ExAC: 12:21331563 A / G
gnomAD v2: 12-21331563-A-G
gnomAD v3: 12-21178629-A-G
gnomAD v4: 12-21178629-A-G
MyVariant Identifiers: chr12:g.21331563A>G (hg19) chr12:g.21178629A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178629A>G , CM000674.2:g.21178629A>G GRCh38
NC_000012.11:g.21331563A>G , CM000674.1:g.21331563A>G GRCh37
NC_000012.10:g.21222830A>G NCBI36
NG_011745.1:g.52436A>G , LRG_1022:g.52436A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.535A>G MANE Select ENSP00000256958.2:p.Met179Val
ENST00000256958.2:c.535A>G ENSP00000256958.2:p.Met179Val
NM_006446.4:c.535A>G , LRG_1022t1:c.535A>G NP_006437.3:p.Met179Val
NM_006446.5:c.535A>G MANE Select NP_006437.3:p.Met179Val
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