Canonical Allele Identifier: CA2633777534
Gene: HSD11B2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67437078del , CM000678.2:g.67437078del GRCh38
NC_000016.9:g.67470981del , CM000678.1:g.67470981del GRCh37
NC_000016.8:g.66028482del NCBI36
NG_011482.1:g.49113del
NG_016549.1:g.10946del

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.*75del MANE Select ENSP00000316786.5:n.*75del
ENST00000326152.5:c.*75del ENSP00000316786.5:n.*75del
NM_000196.3:c.*75del NP_000187.3:n.*75del
NM_000196.4:c.*75del MANE Select NP_000187.3:n.*75del