Canonical Allele Identifier: CA2229309566

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67435985C= , CM000678.2:g.67435985C=	GRCh38
NC_000016.9:g.67469888C= , CM000678.1:g.67469888C=	GRCh37
NC_000016.8:g.66027389C=	NCBI36
NG_016549.1:g.9853C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.507C= MANE Select	ENSP00000316786.5:p.Gly169=
ENST00000326152.5:c.507C=	ENSP00000316786.5:p.Gly169=
ENST00000566606.1:c.485C=	ENSP00000473429.1:n.485C=
ENST00000567684.2:n.370C=
NM_000196.3:c.507C=	NP_000187.3:p.Gly169=
NM_000196.4:c.507C= MANE Select	NP_000187.3:p.Gly169=