Canonical Allele Identifier: CA2229311061
Gene: HSD11B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67437074C= , CM000678.2:g.67437074C= GRCh38
NC_000016.9:g.67470977C= , CM000678.1:g.67470977C= GRCh37
NC_000016.8:g.66028478C= NCBI36
NG_011482.1:g.49113G=
NG_016549.1:g.10942C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.*71C= MANE Select ENSP00000316786.5:n.*71C=
ENST00000326152.5:c.*71C= ENSP00000316786.5:n.*71C=
NM_000196.3:c.*71C= NP_000187.3:n.*71C=
NM_000196.4:c.*71C= MANE Select NP_000187.3:n.*71C=