Canonical Allele Identifier: CA2229309699
Gene: HSD11B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436091C= , CM000678.2:g.67436091C= GRCh38
NC_000016.9:g.67469994C= , CM000678.1:g.67469994C= GRCh37
NC_000016.8:g.66027495C= NCBI36
NG_011482.1:g.50096G=
NG_016549.1:g.9959C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.613C= MANE Select ENSP00000316786.5:p.Pro205=
ENST00000326152.5:c.613C= ENSP00000316786.5:p.Pro205=
ENST00000566606.1:c.591C= ENSP00000473429.1:n.591C=
ENST00000567684.2:n.476C=
NM_000196.3:c.613C= NP_000187.3:p.Pro205=
NM_000196.4:c.613C= MANE Select NP_000187.3:p.Pro205=