Canonical Allele Identifier: CA282323053
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs929635778
gnomAD v3: 16-67436523-AAC-A
gnomAD v4: 16-67436523-AAC-A
MyVariant Identifiers: chr16:g.67470427_67470428del (hg19) chr16:g.67436524_67436525del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436525_67436526del , CM000678.2:g.67436525_67436526del GRCh38
NC_000016.9:g.67470428_67470429del , CM000678.1:g.67470428_67470429del GRCh37
NC_000016.8:g.66027929_66027930del NCBI36
NG_011482.1:g.49662_49663del
NG_016549.1:g.10393_10394del

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.803-63_803-62del MANE Select ENSP00000316786.5:n.803-63_803-62del
ENST00000326152.5:c.803-63_803-62del ENSP00000316786.5:n.803-63_803-62del
NM_000196.3:c.803-63_803-62del NP_000187.3:n.803-63_803-62del
NM_000196.4:c.803-63_803-62del MANE Select NP_000187.3:n.803-63_803-62del
Search 100 bp 5'
Search 100 bp 3'