Canonical Allele Identifier: CA2229309725
Gene: HSD11B2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436109_67436110delinsAG , CM000678.2:g.67436109_67436110delinsAG GRCh38
NC_000016.9:g.67470012_67470013delinsAG , CM000678.1:g.67470012_67470013delinsAG GRCh37
NC_000016.8:g.66027513_66027514delinsAG NCBI36
NG_011482.1:g.50077_50078delinsCT
NG_016549.1:g.9977_9978delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.631_632delinsAG MANE Select ENSP00000316786.5:p.Arg211=
ENST00000326152.5:c.631_632delinsAG ENSP00000316786.5:p.Arg211=
ENST00000566606.1:c.609_610delinsAG ENSP00000473429.1:n.609_610delinsAG
ENST00000567684.2:n.494_495delinsAG
NM_000196.3:c.631_632delinsAG NP_000187.3:p.Arg211=
NM_000196.4:c.631_632delinsAG MANE Select NP_000187.3:p.Arg211=
Search 100 bp 5'
Search 100 bp 3'