Canonical Allele Identifier: CA2229310989
Gene: HSD11B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67437008T= , CM000678.2:g.67437008T= GRCh38
NC_000016.9:g.67470911T= , CM000678.1:g.67470911T= GRCh37
NC_000016.8:g.66028412T= NCBI36
NG_011482.1:g.49179A=
NG_016549.1:g.10876T=

Transcript Alleles

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