Canonical Allele Identifier: CA2229310494
Gene: HSD11B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436697T= , CM000678.2:g.67436697T= GRCh38
NC_000016.9:g.67470600T= , CM000678.1:g.67470600T= GRCh37
NC_000016.8:g.66028101T= NCBI36
NG_011482.1:g.49490A=
NG_016549.1:g.10565T=

Transcript Alleles

HGVS Amino-acid change
ENST00000326152.6:c.912T= MANE Select ENSP00000316786.5:p.His304=
ENST00000326152.5:c.912T= ENSP00000316786.5:p.His304=
NM_000196.3:c.912T= NP_000187.3:p.His304=
NM_000196.4:c.912T= MANE Select NP_000187.3:p.His304=