Canonical Allele Identifier: CA2229309841

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436168A= , CM000678.2:g.67436168A=	GRCh38
NC_000016.9:g.67470071A= , CM000678.1:g.67470071A=	GRCh37
NC_000016.8:g.66027572A=	NCBI36
NG_011482.1:g.50019T=
NG_016549.1:g.10036A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.664+26A= MANE Select	ENSP00000316786.5:n.664+26A=
ENST00000326152.5:c.664+26A=	ENSP00000316786.5:n.664+26A=
ENST00000567684.2:n.527+26A=
NM_000196.3:c.664+26A=	NP_000187.3:n.664+26A=
NM_000196.4:c.664+26A= MANE Select	NP_000187.3:n.664+26A=