Canonical Allele Identifier: CA2229309638

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436047A= , CM000678.2:g.67436047A=	GRCh38
NC_000016.9:g.67469950A= , CM000678.1:g.67469950A=	GRCh37
NC_000016.8:g.66027451A=	NCBI36
NG_011482.1:g.50140T=
NG_016549.1:g.9915A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.569A= MANE Select	ENSP00000316786.5:p.Glu190=
ENST00000326152.5:c.569A=	ENSP00000316786.5:p.Glu190=
ENST00000566606.1:c.547A=	ENSP00000473429.1:n.547A=
ENST00000567684.2:n.432A=
NM_000196.3:c.569A=	NP_000187.3:p.Glu190=
NM_000196.4:c.569A= MANE Select	NP_000187.3:p.Glu190=