Canonical Allele Identifier: CA2229309176

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67435614C= , CM000678.2:g.67435614C=	GRCh38
NC_000016.9:g.67469517C= , CM000678.1:g.67469517C=	GRCh37
NC_000016.8:g.66027018C=	NCBI36
NG_016549.1:g.9482C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.266-14C= MANE Select	ENSP00000316786.5:n.266-14C=
ENST00000326152.5:c.266-14C=	ENSP00000316786.5:n.266-14C=
ENST00000566606.1:c.230C=	ENSP00000473429.1:n.230C=
ENST00000567684.2:n.129-14C=
NM_000196.3:c.266-14C=	NP_000187.3:n.266-14C=
NM_000196.4:c.266-14C= MANE Select	NP_000187.3:n.266-14C=