Canonical Allele Identifier: CA2229309604

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436021A= , CM000678.2:g.67436021A=	GRCh38
NC_000016.9:g.67469924A= , CM000678.1:g.67469924A=	GRCh37
NC_000016.8:g.66027425A=	NCBI36
NG_011482.1:g.50166T=
NG_016549.1:g.9889A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.543A= MANE Select	ENSP00000316786.5:p.Pro181=
ENST00000326152.5:c.543A=	ENSP00000316786.5:p.Pro181=
ENST00000566606.1:c.521A=	ENSP00000473429.1:n.521A=
ENST00000567684.2:n.406A=
NM_000196.3:c.543A=	NP_000187.3:p.Pro181=
NM_000196.4:c.543A= MANE Select	NP_000187.3:p.Pro181=