Canonical Allele Identifier: CA686367857

Gene: SLCO1B1

Linked Data

• dbSNP Id: rs1386934399
• MyVariant Identifiers: chr12:g.21353766_21353767del (hg19) ; chr12:g.21200832_21200833del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21200832_21200833del , CM000674.2:g.21200832_21200833del	GRCh38
NC_000012.11:g.21353766_21353767del , CM000674.1:g.21353766_21353767del	GRCh37
NC_000012.10:g.21245033_21245034del	NCBI36
NG_011745.1:g.74639_74640del , LRG_1022:g.74639_74640del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256958.3:c.1135+160_1135+161del MANE Select	ENSP00000256958.2:n.1135+160_1135+161del
ENST00000256958.2:c.1135+160_1135+161del	ENSP00000256958.2:n.1135+160_1135+161del
NM_006446.4:c.1135+160_1135+161del , LRG_1022t1:c.1135+160_1135+161del	NP_006437.3:n.1135+160_1135+161del
NM_006446.5:c.1135+160_1135+161del MANE Select	NP_006437.3:n.1135+160_1135+161del