Canonical Allele Identifier: CA600282354

Gene: SLCO2B1

Linked Data

• dbSNP Id: rs1359451240
• gnomAD v2: 11-74907592-C-CA
• gnomAD v4: 11-75196547-C-CA
• MyVariant Identifiers: chr11:g.74907592_74907593insA (hg19) ; chr11:g.75196547_75196548insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75196548dup , CM000673.2:g.75196548dup	GRCh38
NC_000011.9:g.74907593dup , CM000673.1:g.74907593dup	GRCh37
NC_000011.8:g.74585241dup	NCBI36
NG_027921.1:g.50562dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1468dup MANE Select	ENSP00000289575.5:p.Met490AsnfsTer12
ENST00000289575.9:c.1468dup	ENSP00000289575.5:p.Met490AsnfsTer12
ENST00000428359.6:c.1402dup	ENSP00000388912.2:p.Met468AsnfsTer12
ENST00000454962.6:c.787dup	ENSP00000389653.2:p.Met263AsnfsTer12
ENST00000525650.5:c.1036dup	ENSP00000436324.1:p.Met346AsnfsTer12
ENST00000528108.1:n.274dup
ENST00000530012.1:n.295dup
ENST00000531756.5:n.1015dup
ENST00000532236.5:c.1120dup	ENSP00000434112.1:p.Met374AsnfsTer12
NM_001145211.2:c.1402dup	NP_001138683.1:p.Met468AsnfsTer12
NM_001145212.2:c.1036dup	NP_001138684.1:p.Met346AsnfsTer12
NM_007256.4:c.1468dup	NP_009187.1:p.Met490AsnfsTer12
XM_017017157.1:c.1474dup	XP_016872646.1:p.Met492AsnfsTer12
NM_001145211.3:c.1402dup	NP_001138683.1:p.Met468AsnfsTer12
NM_001145212.3:c.1036dup	NP_001138684.1:p.Met346AsnfsTer12
NM_007256.5:c.1468dup MANE Select	NP_009187.1:p.Met490AsnfsTer12