Canonical Allele Identifier: CA2576029204
Gene: HSD11B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436422_67436423insGGA , CM000678.2:g.67436422_67436423insGGA GRCh38
NC_000016.9:g.67470325_67470326insGGA , CM000678.1:g.67470325_67470326insGGA GRCh37
NC_000016.8:g.66027826_66027827insGGA NCBI36
NG_011482.1:g.49764_49765insTCC
NG_016549.1:g.10290_10291insGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.802+36_802+37insGGA MANE Select ENSP00000316786.5:n.802+36_802+37insGGA
ENST00000326152.5:c.802+36_802+37insGGA ENSP00000316786.5:n.802+36_802+37insGGA
NM_000196.3:c.802+36_802+37insGGA NP_000187.3:n.802+36_802+37insGGA
NM_000196.4:c.802+36_802+37insGGA MANE Select NP_000187.3:n.802+36_802+37insGGA
Search 100 bp 5'
Search 100 bp 3'