Canonical Allele Identifier: CA2020990611
Gene: SLCO1B1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176837A= , CM000674.2:g.21176837A= GRCh38
NC_000012.11:g.21329771A= , CM000674.1:g.21329771A= GRCh37
NC_000012.10:g.21221038A= NCBI36
NG_011745.1:g.50644A= , LRG_1022:g.50644A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.421A= MANE Select ENSP00000256958.2:p.Thr141=
ENST00000256958.2:c.421A= ENSP00000256958.2:p.Thr141=
ENST00000543498.5:c.487A=
NM_006446.4:c.421A= , LRG_1022t1:c.421A= NP_006437.3:p.Thr141=
NM_006446.5:c.421A= MANE Select NP_006437.3:p.Thr141=
Search 100 bp 5'
Search 100 bp 3'