Canonical Allele Identifier: CA2229309630

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436039C= , CM000678.2:g.67436039C=	GRCh38
NC_000016.9:g.67469942C= , CM000678.1:g.67469942C=	GRCh37
NC_000016.8:g.66027443C=	NCBI36
NG_011482.1:g.50148G=
NG_016549.1:g.9907C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.561C= MANE Select	ENSP00000316786.5:p.Ser187=
ENST00000326152.5:c.561C=	ENSP00000316786.5:p.Ser187=
ENST00000566606.1:c.539C=	ENSP00000473429.1:n.539C=
ENST00000567684.2:n.424C=
NM_000196.3:c.561C=	NP_000187.3:p.Ser187=
NM_000196.4:c.561C= MANE Select	NP_000187.3:p.Ser187=