Canonical Allele Identifier: CA2807429685

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436155_67436156insA , CM000678.2:g.67436155_67436156insA	GRCh38
NC_000016.9:g.67470058_67470059insA , CM000678.1:g.67470058_67470059insA	GRCh37
NC_000016.8:g.66027559_66027560insA	NCBI36
NG_011482.1:g.50031_50032insT
NG_016549.1:g.10023_10024insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.664+13_664+14insA MANE Select	ENSP00000316786.5:n.664+13_664+14insA
ENST00000326152.5:c.664+13_664+14insA	ENSP00000316786.5:n.664+13_664+14insA
ENST00000567684.2:n.527+13_527+14insA
NM_000196.3:c.664+13_664+14insA	NP_000187.3:n.664+13_664+14insA
NM_000196.4:c.664+13_664+14insA MANE Select	NP_000187.3:n.664+13_664+14insA