Canonical Allele Identifier: CA2021001449
Gene: SLCO1B1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200618A= , CM000674.2:g.21200618A= GRCh38
NC_000012.11:g.21353552A= , CM000674.1:g.21353552A= GRCh37
NC_000012.10:g.21244819A= NCBI36
NG_011745.1:g.74425A= , LRG_1022:g.74425A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1081A= MANE Select ENSP00000256958.2:p.Lys361=
ENST00000256958.2:c.1081A= ENSP00000256958.2:p.Lys361=
NM_006446.4:c.1081A= , LRG_1022t1:c.1081A= NP_006437.3:p.Lys361=
NM_006446.5:c.1081A= MANE Select NP_006437.3:p.Lys361=
Search 100 bp 5'
Search 100 bp 3'