Canonical Allele Identifier: CA8110649
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs142435782

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67435971G>A , CM000678.2:g.67435971G>A GRCh38
NC_000016.9:g.67469874G>A , CM000678.1:g.67469874G>A GRCh37
NC_000016.8:g.66027375G>A NCBI36
NG_016549.1:g.9839G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.493G>A MANE Select ENSP00000316786.5:p.Val165Ile
ENST00000326152.5:c.493G>A ENSP00000316786.5:p.Val165Ile
ENST00000566606.1:c.471G>A ENSP00000473429.1:n.471G>A
ENST00000567684.2:n.356G>A
NM_000196.3:c.493G>A NP_000187.3:p.Val165Ile
NM_000196.4:c.493G>A MANE Select NP_000187.3:p.Val165Ile