Canonical Allele Identifier: CA384104956
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs11045819

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176879C>T , CM000674.2:g.21176879C>T GRCh38
NC_000012.11:g.21329813C>T , CM000674.1:g.21329813C>T GRCh37
NC_000012.10:g.21221080C>T NCBI36
NG_011745.1:g.50686C>T , LRG_1022:g.50686C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.463C>T MANE Select ENSP00000256958.2:p.Pro155Ser
ENST00000256958.2:c.463C>T ENSP00000256958.2:p.Pro155Ser
ENST00000543498.5:c.529C>T
NM_006446.4:c.463C>T , LRG_1022t1:c.463C>T NP_006437.3:p.Pro155Ser
NM_006446.5:c.463C>T MANE Select NP_006437.3:p.Pro155Ser