Canonical Allele Identifier: CA2229310387
Gene: HSD11B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436616A= , CM000678.2:g.67436616A= GRCh38
NC_000016.9:g.67470519A= , CM000678.1:g.67470519A= GRCh37
NC_000016.8:g.66028020A= NCBI36
NG_011482.1:g.49571T=
NG_016549.1:g.10484A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.831A= MANE Select ENSP00000316786.5:p.Glu277=
ENST00000326152.5:c.831A= ENSP00000316786.5:p.Glu277=
NM_000196.3:c.831A= NP_000187.3:p.Glu277=
NM_000196.4:c.831A= MANE Select NP_000187.3:p.Glu277=
Search 100 bp 5'
Search 100 bp 3'