Canonical Allele Identifier: CA8110834
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs748368829

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436981C>G , CM000678.2:g.67436981C>G GRCh38
NC_000016.9:g.67470884C>G , CM000678.1:g.67470884C>G GRCh37
NC_000016.8:g.66028385C>G NCBI36
NG_011482.1:g.49206G>C
NG_016549.1:g.10849C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.1196C>G MANE Select ENSP00000316786.5:p.Pro399Arg
ENST00000326152.5:c.1196C>G ENSP00000316786.5:p.Pro399Arg
NM_000196.3:c.1196C>G NP_000187.3:p.Pro399Arg
NM_000196.4:c.1196C>G MANE Select NP_000187.3:p.Pro399Arg