Canonical Allele Identifier: CA2229309862

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436177C= , CM000678.2:g.67436177C=	GRCh38
NC_000016.9:g.67470080C= , CM000678.1:g.67470080C=	GRCh37
NC_000016.8:g.66027581C=	NCBI36
NG_011482.1:g.50010G=
NG_016549.1:g.10045C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.664+35C= MANE Select	ENSP00000316786.5:n.664+35C=
ENST00000326152.5:c.664+35C=	ENSP00000316786.5:n.664+35C=
ENST00000567684.2:n.527+35C=
NM_000196.3:c.664+35C=	NP_000187.3:n.664+35C=
NM_000196.4:c.664+35C= MANE Select	NP_000187.3:n.664+35C=