Canonical Allele Identifier: CA2229309558

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67435982A= , CM000678.2:g.67435982A=	GRCh38
NC_000016.9:g.67469885A= , CM000678.1:g.67469885A=	GRCh37
NC_000016.8:g.66027386A=	NCBI36
NG_016549.1:g.9850A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.504A= MANE Select	ENSP00000316786.5:p.Ala168=
ENST00000326152.5:c.504A=	ENSP00000316786.5:p.Ala168=
ENST00000566606.1:c.482A=	ENSP00000473429.1:n.482A=
ENST00000567684.2:n.367A=
NM_000196.3:c.504A=	NP_000187.3:p.Ala168=
NM_000196.4:c.504A= MANE Select	NP_000187.3:p.Ala168=