Canonical Allele Identifier: CA2229310996
Gene: HSD11B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67437010T= , CM000678.2:g.67437010T= GRCh38
NC_000016.9:g.67470913T= , CM000678.1:g.67470913T= GRCh37
NC_000016.8:g.66028414T= NCBI36
NG_011482.1:g.49177A=
NG_016549.1:g.10878T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.*7T= MANE Select ENSP00000316786.5:n.*7T=
ENST00000326152.5:c.*7T= ENSP00000316786.5:n.*7T=
NM_000196.3:c.*7T= NP_000187.3:n.*7T=
NM_000196.4:c.*7T= MANE Select NP_000187.3:n.*7T=