Canonical Allele Identifier: CA6476662
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs755897728
ExAC: 12:21327663 A / C
gnomAD v2: 12-21327663-A-C
gnomAD v3: 12-21174729-A-C
gnomAD v4: 12-21174729-A-C
MyVariant Identifiers: chr12:g.21327663A>C (hg19) chr12:g.21174729A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174729A>C , CM000674.2:g.21174729A>C GRCh38
NC_000012.11:g.21327663A>C , CM000674.1:g.21327663A>C GRCh37
NC_000012.10:g.21218930A>C NCBI36
NG_011745.1:g.48536A>C , LRG_1022:g.48536A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+20A>C MANE Select ENSP00000256958.2:n.359+20A>C
ENST00000256958.2:c.359+20A>C ENSP00000256958.2:n.359+20A>C
ENST00000543498.5:c.426-2047A>C
NM_006446.4:c.359+20A>C , LRG_1022t1:c.359+20A>C NP_006437.3:n.359+20A>C
NM_006446.5:c.359+20A>C MANE Select NP_006437.3:n.359+20A>C
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