Canonical Allele Identifier: CA2633777547
Gene: HSD11B2 HGNC NCBI

Linked Data

gnomAD v4: 16-67437089-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67437089T>A , CM000678.2:g.67437089T>A GRCh38
NC_000016.9:g.67470992T>A , CM000678.1:g.67470992T>A GRCh37
NC_000016.8:g.66028493T>A NCBI36
NG_011482.1:g.49098A>T
NG_016549.1:g.10957T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.*86T>A MANE Select ENSP00000316786.5:n.*86T>A
ENST00000326152.5:c.*86T>A ENSP00000316786.5:n.*86T>A
NM_000196.3:c.*86T>A NP_000187.3:n.*86T>A
NM_000196.4:c.*86T>A MANE Select NP_000187.3:n.*86T>A
Search 100 bp 5'
Search 100 bp 3'