Canonical Allele Identifier: CA2725844737
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs2121146725

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200803T>G , CM000674.2:g.21200803T>G GRCh38
NC_000012.11:g.21353737T>G , CM000674.1:g.21353737T>G GRCh37
NC_000012.10:g.21245004T>G NCBI36
NG_011745.1:g.74610T>G , LRG_1022:g.74610T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1135+131T>G MANE Select ENSP00000256958.2:n.1135+131T>G
ENST00000256958.2:c.1135+131T>G ENSP00000256958.2:n.1135+131T>G
NM_006446.4:c.1135+131T>G , LRG_1022t1:c.1135+131T>G NP_006437.3:n.1135+131T>G
NM_006446.5:c.1135+131T>G MANE Select NP_006437.3:n.1135+131T>G