Canonical Allele Identifier: CA2576029156
Gene: HSD11B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436007dup , CM000678.2:g.67436007dup GRCh38
NC_000016.9:g.67469910dup , CM000678.1:g.67469910dup GRCh37
NC_000016.8:g.66027411dup NCBI36
NG_016549.1:g.9875dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.529dup MANE Select ENSP00000316786.5:p.Ala177GlyfsTer11
ENST00000326152.5:c.529dup ENSP00000316786.5:p.Ala177GlyfsTer11
ENST00000566606.1:c.507dup ENSP00000473429.1:n.507dup
ENST00000567684.2:n.392dup
NM_000196.3:c.529dup NP_000187.3:p.Ala177GlyfsTer11
NM_000196.4:c.529dup MANE Select NP_000187.3:p.Ala177GlyfsTer11
Search 100 bp 5'
Search 100 bp 3'