Canonical Allele Identifier: CA2020991452
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178629A= , CM000674.2:g.21178629A= GRCh38
NC_000012.11:g.21331563A= , CM000674.1:g.21331563A= GRCh37
NC_000012.10:g.21222830A= NCBI36
NG_011745.1:g.52436A= , LRG_1022:g.52436A=

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.535A= MANE Select ENSP00000256958.2:p.Met179=
ENST00000256958.2:c.535A= ENSP00000256958.2:p.Met179=
NM_006446.4:c.535A= , LRG_1022t1:c.535A= NP_006437.3:p.Met179=
NM_006446.5:c.535A= MANE Select NP_006437.3:p.Met179=