Canonical Allele Identifier: CA723037278
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs1480606855
gnomAD v3: 16-67436505-C-CA
gnomAD v4: 16-67436505-C-CA
MyVariant Identifiers: chr16:g.67470408_67470409insA (hg19) chr16:g.67436505_67436506insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436506dup , CM000678.2:g.67436506dup GRCh38
NC_000016.9:g.67470409dup , CM000678.1:g.67470409dup GRCh37
NC_000016.8:g.66027910dup NCBI36
NG_011482.1:g.49681dup
NG_016549.1:g.10374dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.803-82dup MANE Select ENSP00000316786.5:n.803-82dup
ENST00000326152.5:c.803-82dup ENSP00000316786.5:n.803-82dup
NM_000196.3:c.803-82dup NP_000187.3:n.803-82dup
NM_000196.4:c.803-82dup MANE Select NP_000187.3:n.803-82dup
Search 100 bp 5'
Search 100 bp 3'