Canonical Allele Identifier: CA2229309613

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436030T= , CM000678.2:g.67436030T=	GRCh38
NC_000016.9:g.67469933T= , CM000678.1:g.67469933T=	GRCh37
NC_000016.8:g.66027434T=	NCBI36
NG_011482.1:g.50157A=
NG_016549.1:g.9898T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.552T= MANE Select	ENSP00000316786.5:p.Thr184=
ENST00000326152.5:c.552T=	ENSP00000316786.5:p.Thr184=
ENST00000566606.1:c.530T=	ENSP00000473429.1:n.530T=
ENST00000567684.2:n.415T=
NM_000196.3:c.552T=	NP_000187.3:p.Thr184=
NM_000196.4:c.552T= MANE Select	NP_000187.3:p.Thr184=