Canonical Allele Identifier: CA2229309748
Gene: HSD11B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436124A= , CM000678.2:g.67436124A= GRCh38
NC_000016.9:g.67470027A= , CM000678.1:g.67470027A= GRCh37
NC_000016.8:g.66027528A= NCBI36
NG_011482.1:g.50063T=
NG_016549.1:g.9992A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.646A= MANE Select ENSP00000316786.5:p.Thr216=
ENST00000326152.5:c.646A= ENSP00000316786.5:p.Thr216=
ENST00000566606.1:c.624A= ENSP00000473429.1:n.624A=
ENST00000567684.2:n.509A=
NM_000196.3:c.646A= NP_000187.3:p.Thr216=
NM_000196.4:c.646A= MANE Select NP_000187.3:p.Thr216=