Canonical Allele Identifier: CA2229309833

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436162G= , CM000678.2:g.67436162G=	GRCh38
NC_000016.9:g.67470065G= , CM000678.1:g.67470065G=	GRCh37
NC_000016.8:g.66027566G=	NCBI36
NG_011482.1:g.50025C=
NG_016549.1:g.10030G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.664+20G= MANE Select	ENSP00000316786.5:n.664+20G=
ENST00000326152.5:c.664+20G=	ENSP00000316786.5:n.664+20G=
ENST00000567684.2:n.527+20G=
NM_000196.3:c.664+20G=	NP_000187.3:n.664+20G=
NM_000196.4:c.664+20G= MANE Select	NP_000187.3:n.664+20G=