Canonical Allele Identifier: CA8110849
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs574787024

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67437042G>A , CM000678.2:g.67437042G>A GRCh38
NC_000016.9:g.67470945G>A , CM000678.1:g.67470945G>A GRCh37
NC_000016.8:g.66028446G>A NCBI36
NG_011482.1:g.49145C>T
NG_016549.1:g.10910G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.*39G>A MANE Select ENSP00000316786.5:n.*39G>A
ENST00000326152.5:c.*39G>A ENSP00000316786.5:n.*39G>A
NM_000196.3:c.*39G>A NP_000187.3:n.*39G>A
NM_000196.4:c.*39G>A MANE Select NP_000187.3:n.*39G>A