Canonical Allele Identifier: CA2021001379
Gene: SLCO1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200498A= , CM000674.2:g.21200498A= GRCh38
NC_000012.11:g.21353432A= , CM000674.1:g.21353432A= GRCh37
NC_000012.10:g.21244699A= NCBI36
NG_011745.1:g.74305A= , LRG_1022:g.74305A=

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.971-10A= MANE Select ENSP00000256958.2:n.971-10A=
ENST00000256958.2:c.971-10A= ENSP00000256958.2:n.971-10A=
NM_006446.4:c.971-10A= , LRG_1022t1:c.971-10A= NP_006437.3:n.971-10A=
NM_006446.5:c.971-10A= MANE Select NP_006437.3:n.971-10A=