Canonical Allele Identifier: CA2229311006
Gene: HSD11B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67437013A= , CM000678.2:g.67437013A= GRCh38
NC_000016.9:g.67470916A= , CM000678.1:g.67470916A= GRCh37
NC_000016.8:g.66028417A= NCBI36
NG_011482.1:g.49174T=
NG_016549.1:g.10881A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.*10A= MANE Select ENSP00000316786.5:n.*10A=
ENST00000326152.5:c.*10A= ENSP00000316786.5:n.*10A=
NM_000196.3:c.*10A= NP_000187.3:n.*10A=
NM_000196.4:c.*10A= MANE Select NP_000187.3:n.*10A=