Canonical Allele Identifier: CA2633777543
Gene: HSD11B2 HGNC NCBI

Linked Data

gnomAD v4: 16-67437082-AT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67437084del , CM000678.2:g.67437084del GRCh38
NC_000016.9:g.67470987del , CM000678.1:g.67470987del GRCh37
NC_000016.8:g.66028488del NCBI36
NG_011482.1:g.49104del
NG_016549.1:g.10952del

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.*81del MANE Select ENSP00000316786.5:n.*81del
ENST00000326152.5:c.*81del ENSP00000316786.5:n.*81del
NM_000196.3:c.*81del NP_000187.3:n.*81del
NM_000196.4:c.*81del MANE Select NP_000187.3:n.*81del
Search 100 bp 5'
Search 100 bp 3'