Canonical Allele Identifier: CA2229310453
Gene: HSD11B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436677G= , CM000678.2:g.67436677G= GRCh38
NC_000016.9:g.67470580G= , CM000678.1:g.67470580G= GRCh37
NC_000016.8:g.66028081G= NCBI36
NG_011482.1:g.49510C=
NG_016549.1:g.10545G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.892G= MANE Select ENSP00000316786.5:p.Asp298=
ENST00000326152.5:c.892G= ENSP00000316786.5:p.Asp298=
NM_000196.3:c.892G= NP_000187.3:p.Asp298=
NM_000196.4:c.892G= MANE Select NP_000187.3:p.Asp298=
Search 100 bp 5'
Search 100 bp 3'