Canonical Allele Identifier: CA2617895399
Gene: SLCO1B1 HGNC NCBI

Linked Data

gnomAD v4: 12-21200403-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200403G>T , CM000674.2:g.21200403G>T GRCh38
NC_000012.11:g.21353337G>T , CM000674.1:g.21353337G>T GRCh37
NC_000012.10:g.21244604G>T NCBI36
NG_011745.1:g.74210G>T , LRG_1022:g.74210G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.971-105G>T MANE Select ENSP00000256958.2:n.971-105G>T
ENST00000256958.2:c.971-105G>T ENSP00000256958.2:n.971-105G>T
NM_006446.4:c.971-105G>T , LRG_1022t1:c.971-105G>T NP_006437.3:n.971-105G>T
NM_006446.5:c.971-105G>T MANE Select NP_006437.3:n.971-105G>T
Search 100 bp 5'
Search 100 bp 3'