Canonical Allele Identifier: CA224625049

Gene: SLCO2B1

Linked Data

• dbSNP Id: rs141281678
• gnomAD v3: 11-75190500-A-G
• gnomAD v4: 11-75190500-A-G
• MyVariant Identifiers: chr11:g.74901545A>G (hg19) ; chr11:g.75190500A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75190500A>G , CM000673.2:g.75190500A>G	GRCh38
NC_000011.9:g.74901545A>G , CM000673.1:g.74901545A>G	GRCh37
NC_000011.8:g.74579193A>G	NCBI36
NG_027921.1:g.44514A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1075+2262A>G MANE Select	ENSP00000289575.5:n.1075+2262A>G
ENST00000289575.9:c.1075+2262A>G	ENSP00000289575.5:n.1075+2262A>G
ENST00000428359.6:c.1009+2262A>G	ENSP00000388912.2:n.1009+2262A>G
ENST00000454962.6:c.394+2262A>G	ENSP00000389653.2:n.394+2262A>G
ENST00000525650.5:c.643+2262A>G	ENSP00000436324.1:n.643+2262A>G
ENST00000531756.5:n.622+2262A>G
ENST00000532236.5:c.727+2262A>G	ENSP00000434112.1:n.727+2262A>G
NM_001145211.2:c.1009+2262A>G	NP_001138683.1:n.1009+2262A>G
NM_001145212.2:c.643+2262A>G	NP_001138684.1:n.643+2262A>G
NM_007256.4:c.1075+2262A>G	NP_009187.1:n.1075+2262A>G
XM_017017157.1:c.1081+2262A>G	XP_016872646.1:n.1081+2262A>G
NM_001145211.3:c.1009+2262A>G	NP_001138683.1:n.1009+2262A>G
NM_001145212.3:c.643+2262A>G	NP_001138684.1:n.643+2262A>G
NM_007256.5:c.1075+2262A>G MANE Select	NP_009187.1:n.1075+2262A>G