Canonical Allele Identifier: CA2229309141

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67435569G= , CM000678.2:g.67435569G=	GRCh38
NC_000016.9:g.67469472G= , CM000678.1:g.67469472G=	GRCh37
NC_000016.8:g.66026973G=	NCBI36
NG_016549.1:g.9437G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.266-59G= MANE Select	ENSP00000316786.5:n.266-59G=
ENST00000326152.5:c.266-59G=	ENSP00000316786.5:n.266-59G=
ENST00000566606.1:c.185G=	ENSP00000473429.1:n.185G=
ENST00000567684.2:n.129-59G=
NM_000196.3:c.266-59G=	NP_000187.3:n.266-59G=
NM_000196.4:c.266-59G= MANE Select	NP_000187.3:n.266-59G=