Canonical Allele Identifier: CA2229309654
Gene: HSD11B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436063C= , CM000678.2:g.67436063C= GRCh38
NC_000016.9:g.67469966C= , CM000678.1:g.67469966C= GRCh37
NC_000016.8:g.66027467C= NCBI36
NG_011482.1:g.50124G=
NG_016549.1:g.9931C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.585C= MANE Select ENSP00000316786.5:p.Gly195=
ENST00000326152.5:c.585C= ENSP00000316786.5:p.Gly195=
ENST00000566606.1:c.563C= ENSP00000473429.1:n.563C=
ENST00000567684.2:n.448C=
NM_000196.3:c.585C= NP_000187.3:p.Gly195=
NM_000196.4:c.585C= MANE Select NP_000187.3:p.Gly195=