Canonical Allele Identifier: CA2229309204

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67435647C= , CM000678.2:g.67435647C=	GRCh38
NC_000016.9:g.67469550C= , CM000678.1:g.67469550C=	GRCh37
NC_000016.8:g.66027051C=	NCBI36
NG_016549.1:g.9515C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.285C= MANE Select	ENSP00000316786.5:p.Gly95=
ENST00000326152.5:c.285C=	ENSP00000316786.5:p.Gly95=
ENST00000566606.1:c.263C=	ENSP00000473429.1:n.263C=
ENST00000567684.2:n.148C=
NM_000196.3:c.285C=	NP_000187.3:p.Gly95=
NM_000196.4:c.285C= MANE Select	NP_000187.3:p.Gly95=