Canonical Allele Identifier: CA2229310271

Gene: HSD11B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436491_67436494delinsTGTA , CM000678.2:g.67436491_67436494delinsTGTA	GRCh38
NC_000016.9:g.67470394_67470397delinsTGTA , CM000678.1:g.67470394_67470397delinsTGTA	GRCh37
NC_000016.8:g.66027895_66027898delinsTGTA	NCBI36
NG_011482.1:g.49693_49696delinsTACA
NG_016549.1:g.10359_10362delinsTGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.803-97_803-94delinsTGTA MANE Select	ENSP00000316786.5:n.803-97_803-94delinsTGTA
ENST00000326152.5:c.803-97_803-94delinsTGTA	ENSP00000316786.5:n.803-97_803-94delinsTGTA
NM_000196.3:c.803-97_803-94delinsTGTA	NP_000187.3:n.803-97_803-94delinsTGTA
NM_000196.4:c.803-97_803-94delinsTGTA MANE Select	NP_000187.3:n.803-97_803-94delinsTGTA