Canonical Allele Identifier: CA603657601
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1240072820
gnomAD v2: 12-21327954-G-C
gnomAD v3: 12-21175020-G-C
gnomAD v4: 12-21175020-G-C
MyVariant Identifiers: chr12:g.21327954G>C (hg19) chr12:g.21175020G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21175020G>C , CM000674.2:g.21175020G>C GRCh38
NC_000012.11:g.21327954G>C , CM000674.1:g.21327954G>C GRCh37
NC_000012.10:g.21219221G>C NCBI36
NG_011745.1:g.48827G>C , LRG_1022:g.48827G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+311G>C MANE Select ENSP00000256958.2:n.359+311G>C
ENST00000256958.2:c.359+311G>C ENSP00000256958.2:n.359+311G>C
ENST00000543498.5:c.426-1756G>C
NM_006446.4:c.359+311G>C , LRG_1022t1:c.359+311G>C NP_006437.3:n.359+311G>C
NM_006446.5:c.359+311G>C MANE Select NP_006437.3:n.359+311G>C
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