Canonical Allele Identifier: CA2020991453
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178630T= , CM000674.2:g.21178630T= GRCh38
NC_000012.11:g.21331564T= , CM000674.1:g.21331564T= GRCh37
NC_000012.10:g.21222831T= NCBI36
NG_011745.1:g.52437T= , LRG_1022:g.52437T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.536T= MANE Select ENSP00000256958.2:p.Met179=
ENST00000256958.2:c.536T= ENSP00000256958.2:p.Met179=
NM_006446.4:c.536T= , LRG_1022t1:c.536T= NP_006437.3:p.Met179=
NM_006446.5:c.536T= MANE Select NP_006437.3:p.Met179=