Canonical Allele Identifier: CA2229310379
Gene: HSD11B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436605G= , CM000678.2:g.67436605G= GRCh38
NC_000016.9:g.67470508G= , CM000678.1:g.67470508G= GRCh37
NC_000016.8:g.66028009G= NCBI36
NG_011482.1:g.49582C=
NG_016549.1:g.10473G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.820G= MANE Select ENSP00000316786.5:p.Gly274=
ENST00000326152.5:c.820G= ENSP00000316786.5:p.Gly274=
NM_000196.3:c.820G= NP_000187.3:p.Gly274=
NM_000196.4:c.820G= MANE Select NP_000187.3:p.Gly274=
Search 100 bp 5'
Search 100 bp 3'