Canonical Allele Identifier: CA8110757
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs759849379

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436588A>G , CM000678.2:g.67436588A>G GRCh38
NC_000016.9:g.67470491A>G , CM000678.1:g.67470491A>G GRCh37
NC_000016.8:g.66027992A>G NCBI36
NG_011482.1:g.49599T>C
NG_016549.1:g.10456A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000326152.6:c.803A>G MANE Select ENSP00000316786.5:p.Glu268Gly
ENST00000326152.5:c.803A>G ENSP00000316786.5:p.Glu268Gly
NM_000196.3:c.803A>G NP_000187.3:p.Glu268Gly
NM_000196.4:c.803A>G MANE Select NP_000187.3:p.Glu268Gly