Canonical Allele Identifier: CA2020999786
Gene: SLCO1B1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21196811T= , CM000674.2:g.21196811T= GRCh38
NC_000012.11:g.21349745T= , CM000674.1:g.21349745T= GRCh37
NC_000012.10:g.21241012T= NCBI36
NG_011745.1:g.70618T= , LRG_1022:g.70618T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.728-135T= MANE Select ENSP00000256958.2:n.728-135T=
ENST00000256958.2:c.728-135T= ENSP00000256958.2:n.728-135T=
NM_006446.4:c.728-135T= , LRG_1022t1:c.728-135T= NP_006437.3:n.728-135T=
NM_006446.5:c.728-135T= MANE Select NP_006437.3:n.728-135T=
Search 100 bp 5'
Search 100 bp 3'