Canonical Allele Identifier: CA6476672
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs776785374

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176800T>C , CM000674.2:g.21176800T>C GRCh38
NC_000012.11:g.21329734T>C , CM000674.1:g.21329734T>C GRCh37
NC_000012.10:g.21221001T>C NCBI36
NG_011745.1:g.50607T>C , LRG_1022:g.50607T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.384T>C MANE Select ENSP00000256958.2:p.Asn128=
ENST00000256958.2:c.384T>C ENSP00000256958.2:p.Asn128=
ENST00000543498.5:c.450T>C
NM_006446.4:c.384T>C , LRG_1022t1:c.384T>C NP_006437.3:p.Asn128=
NM_006446.5:c.384T>C MANE Select NP_006437.3:p.Asn128=