Canonical Allele Identifier: CA2021009759
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21216093A= , CM000674.2:g.21216093A= GRCh38
NC_000012.11:g.21369027A= , CM000674.1:g.21369027A= GRCh37
NC_000012.10:g.21260294A= NCBI36
NG_011745.1:g.89900A= , LRG_1022:g.89900A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1498-1026A= MANE Select ENSP00000256958.2:n.1498-1026A=
ENST00000256958.2:c.1498-1026A= ENSP00000256958.2:n.1498-1026A=
NM_006446.4:c.1498-1026A= , LRG_1022t1:c.1498-1026A= NP_006437.3:n.1498-1026A=
NM_006446.5:c.1498-1026A= MANE Select NP_006437.3:n.1498-1026A=