Canonical Allele Identifier: CA2229309572

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67435990A= , CM000678.2:g.67435990A=	GRCh38
NC_000016.9:g.67469893A= , CM000678.1:g.67469893A=	GRCh37
NC_000016.8:g.66027394A=	NCBI36
NG_016549.1:g.9858A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.512A= MANE Select	ENSP00000316786.5:p.Asn171=
ENST00000326152.5:c.512A=	ENSP00000316786.5:p.Asn171=
ENST00000566606.1:c.490A=	ENSP00000473429.1:n.490A=
ENST00000567684.2:n.375A=
NM_000196.3:c.512A=	NP_000187.3:p.Asn171=
NM_000196.4:c.512A= MANE Select	NP_000187.3:p.Asn171=