Canonical Allele Identifier: CA2229310267
Gene: HSD11B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436491T= , CM000678.2:g.67436491T= GRCh38
NC_000016.9:g.67470394T= , CM000678.1:g.67470394T= GRCh37
NC_000016.8:g.66027895T= NCBI36
NG_011482.1:g.49696A=
NG_016549.1:g.10359T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.803-97T= MANE Select ENSP00000316786.5:n.803-97T=
ENST00000326152.5:c.803-97T= ENSP00000316786.5:n.803-97T=
NM_000196.3:c.803-97T= NP_000187.3:n.803-97T=
NM_000196.4:c.803-97T= MANE Select NP_000187.3:n.803-97T=