Canonical Allele Identifier: CA2229309585

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67435996T= , CM000678.2:g.67435996T=	GRCh38
NC_000016.9:g.67469899T= , CM000678.1:g.67469899T=	GRCh37
NC_000016.8:g.66027400T=	NCBI36
NG_016549.1:g.9864T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.518T= MANE Select	ENSP00000316786.5:p.Val173=
ENST00000326152.5:c.518T=	ENSP00000316786.5:p.Val173=
ENST00000566606.1:c.496T=	ENSP00000473429.1:n.496T=
ENST00000567684.2:n.381T=
NM_000196.3:c.518T=	NP_000187.3:p.Val173=
NM_000196.4:c.518T= MANE Select	NP_000187.3:p.Val173=