Canonical Allele Identifier: CA2229310301

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436526A= , CM000678.2:g.67436526A=	GRCh38
NC_000016.9:g.67470429A= , CM000678.1:g.67470429A=	GRCh37
NC_000016.8:g.66027930A=	NCBI36
NG_011482.1:g.49661T=
NG_016549.1:g.10394A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000326152.6:c.803-62A= MANE Select	ENSP00000316786.5:n.803-62A=
ENST00000326152.5:c.803-62A=	ENSP00000316786.5:n.803-62A=
NM_000196.3:c.803-62A=	NP_000187.3:n.803-62A=
NM_000196.4:c.803-62A= MANE Select	NP_000187.3:n.803-62A=