Canonical Allele Identifier: CA2229309556

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67435980G= , CM000678.2:g.67435980G=	GRCh38
NC_000016.9:g.67469883G= , CM000678.1:g.67469883G=	GRCh37
NC_000016.8:g.66027384G=	NCBI36
NG_016549.1:g.9848G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.502G= MANE Select	ENSP00000316786.5:p.Ala168=
ENST00000326152.5:c.502G=	ENSP00000316786.5:p.Ala168=
ENST00000566606.1:c.480G=	ENSP00000473429.1:n.480G=
ENST00000567684.2:n.365G=
NM_000196.3:c.502G=	NP_000187.3:p.Ala168=
NM_000196.4:c.502G= MANE Select	NP_000187.3:p.Ala168=