Canonical Allele Identifier: CA2633777548
Gene: HSD11B2 HGNC NCBI

Linked Data

gnomAD v4: 16-67437089-T-TC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67437094dup , CM000678.2:g.67437094dup GRCh38
NC_000016.9:g.67470997dup , CM000678.1:g.67470997dup GRCh37
NC_000016.8:g.66028498dup NCBI36
NG_011482.1:g.49097dup
NG_016549.1:g.10962dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.*91dup MANE Select ENSP00000316786.5:n.*91dup
ENST00000326152.5:c.*91dup ENSP00000316786.5:n.*91dup
NM_000196.3:c.*91dup NP_000187.3:n.*91dup
NM_000196.4:c.*91dup MANE Select NP_000187.3:n.*91dup
Search 100 bp 5'
Search 100 bp 3'