Canonical Allele Identifier: CA396281411
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs1567530663

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436386G>A , CM000678.2:g.67436386G>A GRCh38
NC_000016.9:g.67470289G>A , CM000678.1:g.67470289G>A GRCh37
NC_000016.8:g.66027790G>A NCBI36
NG_011482.1:g.49801C>T
NG_016549.1:g.10254G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.802G>A MANE Select ENSP00000316786.5:p.Glu268Lys
ENST00000326152.5:c.802G>A ENSP00000316786.5:p.Glu268Lys
NM_000196.3:c.802G>A NP_000187.3:p.Glu268Lys
NM_000196.4:c.802G>A MANE Select NP_000187.3:p.Glu268Lys