Canonical Allele Identifier: CA2229309751
Gene: HSD11B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436127G= , CM000678.2:g.67436127G= GRCh38
NC_000016.9:g.67470030G= , CM000678.1:g.67470030G= GRCh37
NC_000016.8:g.66027531G= NCBI36
NG_011482.1:g.50060C=
NG_016549.1:g.9995G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.649G= MANE Select ENSP00000316786.5:p.Val217=
ENST00000326152.5:c.649G= ENSP00000316786.5:p.Val217=
ENST00000566606.1:c.627G= ENSP00000473429.1:n.627G=
ENST00000567684.2:n.512G=
NM_000196.3:c.649G= NP_000187.3:p.Val217=
NM_000196.4:c.649G= MANE Select NP_000187.3:p.Val217=