Canonical Allele Identifier: CA2229310272

Gene: HSD11B2

Linked Data

• dbSNP Id: rs2040974669

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436494_67436496del , CM000678.2:g.67436494_67436496del	GRCh38
NC_000016.9:g.67470397_67470399del , CM000678.1:g.67470397_67470399del	GRCh37
NC_000016.8:g.66027898_66027900del	NCBI36
NG_011482.1:g.49693_49695del
NG_016549.1:g.10362_10364del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.803-94_803-92del MANE Select	ENSP00000316786.5:n.803-94_803-92del
ENST00000326152.5:c.803-94_803-92del	ENSP00000316786.5:n.803-94_803-92del
NM_000196.3:c.803-94_803-92del	NP_000187.3:n.803-94_803-92del
NM_000196.4:c.803-94_803-92del MANE Select	NP_000187.3:n.803-94_803-92del