Canonical Allele Identifier: CA2021001489
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200693G= , CM000674.2:g.21200693G= GRCh38
NC_000012.11:g.21353627G= , CM000674.1:g.21353627G= GRCh37
NC_000012.10:g.21244894G= NCBI36
NG_011745.1:g.74500G= , LRG_1022:g.74500G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1135+21G= MANE Select ENSP00000256958.2:n.1135+21G=
ENST00000256958.2:c.1135+21G= ENSP00000256958.2:n.1135+21G=
NM_006446.4:c.1135+21G= , LRG_1022t1:c.1135+21G= NP_006437.3:n.1135+21G=
NM_006446.5:c.1135+21G= MANE Select NP_006437.3:n.1135+21G=