Canonical Allele Identifier: CA2807429757
Gene: HSD11B2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436423_67436424insGTGGGGTGGGGGTGGGG , CM000678.2:g.67436423_67436424insGTGGGGTGGGGGTGGGG GRCh38
NC_000016.9:g.67470326_67470327insGTGGGGTGGGGGTGGGG , CM000678.1:g.67470326_67470327insGTGGGGTGGGGGTGGGG GRCh37
NC_000016.8:g.66027827_66027828insGTGGGGTGGGGGTGGGG NCBI36
NG_011482.1:g.49763_49764insCCCCACCCCCACCCCAC
NG_016549.1:g.10291_10292insGTGGGGTGGGGGTGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.802+37_802+38insGTGGGGTGGGGGTGGGG MANE Select ENSP00000316786.5:n.802+37_802+38insGTGGGGTGGGGGTGGGG
ENST00000326152.5:c.802+37_802+38insGTGGGGTGGGGGTGGGG ENSP00000316786.5:n.802+37_802+38insGTGGGGTGGGGGTGGGG
NM_000196.3:c.802+37_802+38insGTGGGGTGGGGGTGGGG NP_000187.3:n.802+37_802+38insGTGGGGTGGGGGTGGGG
NM_000196.4:c.802+37_802+38insGTGGGGTGGGGGTGGGG MANE Select NP_000187.3:n.802+37_802+38insGTGGGGTGGGGGTGGGG
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