Canonical Allele Identifier: CA2229309597

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436012G= , CM000678.2:g.67436012G=	GRCh38
NC_000016.9:g.67469915G= , CM000678.1:g.67469915G=	GRCh37
NC_000016.8:g.66027416G=	NCBI36
NG_016549.1:g.9880G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.534G= MANE Select	ENSP00000316786.5:p.Glu178=
ENST00000326152.5:c.534G=	ENSP00000316786.5:p.Glu178=
ENST00000566606.1:c.512G=	ENSP00000473429.1:n.512G=
ENST00000567684.2:n.397G=
NM_000196.3:c.534G=	NP_000187.3:p.Glu178=
NM_000196.4:c.534G= MANE Select	NP_000187.3:p.Glu178=