Canonical Allele Identifier: CA2229309739
Gene: HSD11B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436119T= , CM000678.2:g.67436119T= GRCh38
NC_000016.9:g.67470022T= , CM000678.1:g.67470022T= GRCh37
NC_000016.8:g.66027523T= NCBI36
NG_011482.1:g.50068A=
NG_016549.1:g.9987T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.641T= MANE Select ENSP00000316786.5:p.Ile214=
ENST00000326152.5:c.641T= ENSP00000316786.5:p.Ile214=
ENST00000566606.1:c.619T= ENSP00000473429.1:n.619T=
ENST00000567684.2:n.504T=
NM_000196.3:c.641T= NP_000187.3:p.Ile214=
NM_000196.4:c.641T= MANE Select NP_000187.3:p.Ile214=