Canonical Allele Identifier: CA2576029207
Gene: HSD11B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436425dup , CM000678.2:g.67436425dup GRCh38
NC_000016.9:g.67470328dup , CM000678.1:g.67470328dup GRCh37
NC_000016.8:g.66027829dup NCBI36
NG_011482.1:g.49762dup
NG_016549.1:g.10293dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.802+39dup MANE Select ENSP00000316786.5:n.802+39dup
ENST00000326152.5:c.802+39dup ENSP00000316786.5:n.802+39dup
NM_000196.3:c.802+39dup NP_000187.3:n.802+39dup
NM_000196.4:c.802+39dup MANE Select NP_000187.3:n.802+39dup
Search 100 bp 5'
Search 100 bp 3'