Canonical Allele Identifier: CA2229310331
Gene: HSD11B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436567_67436568delinsAC , CM000678.2:g.67436567_67436568delinsAC GRCh38
NC_000016.9:g.67470470_67470471delinsAC , CM000678.1:g.67470470_67470471delinsAC GRCh37
NC_000016.8:g.66027971_66027972delinsAC NCBI36
NG_011482.1:g.49619_49620delinsGT
NG_016549.1:g.10435_10436delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.803-21_803-20delinsAC MANE Select ENSP00000316786.5:n.803-21_803-20delinsAC
ENST00000326152.5:c.803-21_803-20delinsAC ENSP00000316786.5:n.803-21_803-20delinsAC
NM_000196.3:c.803-21_803-20delinsAC NP_000187.3:n.803-21_803-20delinsAC
NM_000196.4:c.803-21_803-20delinsAC MANE Select NP_000187.3:n.803-21_803-20delinsAC
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