Canonical Allele Identifier: CA2020991342
Gene: SLCO1B1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178439G= , CM000674.2:g.21178439G= GRCh38
NC_000012.11:g.21331373G= , CM000674.1:g.21331373G= GRCh37
NC_000012.10:g.21222640G= NCBI36
NG_011745.1:g.52246G= , LRG_1022:g.52246G=

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.482-137G= MANE Select ENSP00000256958.2:n.482-137G=
ENST00000256958.2:c.482-137G= ENSP00000256958.2:n.482-137G=
NM_006446.4:c.482-137G= , LRG_1022t1:c.482-137G= NP_006437.3:n.482-137G=
NM_006446.5:c.482-137G= MANE Select NP_006437.3:n.482-137G=
Search 100 bp 5'
Search 100 bp 3'