Canonical Allele Identifier: CA2229309589

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436007G= , CM000678.2:g.67436007G=	GRCh38
NC_000016.9:g.67469910G= , CM000678.1:g.67469910G=	GRCh37
NC_000016.8:g.66027411G=	NCBI36
NG_016549.1:g.9875G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.529G= MANE Select	ENSP00000316786.5:p.Ala177=
ENST00000326152.5:c.529G=	ENSP00000316786.5:p.Ala177=
ENST00000566606.1:c.507G=	ENSP00000473429.1:n.507G=
ENST00000567684.2:n.392G=
NM_000196.3:c.529G=	NP_000187.3:p.Ala177=
NM_000196.4:c.529G= MANE Select	NP_000187.3:p.Ala177=