Canonical Allele Identifier: CA384106696
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs972134088
gnomAD v2: 12-21353541-C-T
gnomAD v4: 12-21200607-C-T
MyVariant Identifiers: chr12:g.21353541C>T (hg19) chr12:g.21200607C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200607C>T , CM000674.2:g.21200607C>T GRCh38
NC_000012.11:g.21353541C>T , CM000674.1:g.21353541C>T GRCh37
NC_000012.10:g.21244808C>T NCBI36
NG_011745.1:g.74414C>T , LRG_1022:g.74414C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.1070C>T MANE Select ENSP00000256958.2:p.Thr357Ile
ENST00000256958.2:c.1070C>T ENSP00000256958.2:p.Thr357Ile
NM_006446.4:c.1070C>T , LRG_1022t1:c.1070C>T NP_006437.3:p.Thr357Ile
NM_006446.5:c.1070C>T MANE Select NP_006437.3:p.Thr357Ile
Search 100 bp 5'
Search 100 bp 3'