Canonical Allele Identifier: CA2229310918
Gene: HSD11B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436956C= , CM000678.2:g.67436956C= GRCh38
NC_000016.9:g.67470859C= , CM000678.1:g.67470859C= GRCh37
NC_000016.8:g.66028360C= NCBI36
NG_011482.1:g.49231G=
NG_016549.1:g.10824C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.1171C= MANE Select ENSP00000316786.5:p.Gln391=
ENST00000326152.5:c.1171C= ENSP00000316786.5:p.Gln391=
NM_000196.3:c.1171C= NP_000187.3:p.Gln391=
NM_000196.4:c.1171C= MANE Select NP_000187.3:p.Gln391=