Canonical Allele Identifier: CA2633780219
Gene: HSD11B2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436588_67436589del , CM000678.2:g.67436588_67436589del GRCh38
NC_000016.9:g.67470491_67470492del , CM000678.1:g.67470491_67470492del GRCh37
NC_000016.8:g.66027992_66027993del NCBI36
NG_011482.1:g.49600_49601del
NG_016549.1:g.10456_10457del

Transcript Alleles

HGVS Amino-acid change
ENST00000326152.6:c.803_804del
ENST00000326152.5:c.803_804del
NM_000196.3:c.803_804del
NM_000196.4:c.803_804del