Canonical Allele Identifier: CA8110769
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs753129876

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436685C>A , CM000678.2:g.67436685C>A GRCh38
NC_000016.9:g.67470588C>A , CM000678.1:g.67470588C>A GRCh37
NC_000016.8:g.66028089C>A NCBI36
NG_011482.1:g.49502G>T
NG_016549.1:g.10553C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000326152.6:c.900C>A MANE Select ENSP00000316786.5:p.Ile300=
ENST00000326152.5:c.900C>A ENSP00000316786.5:p.Ile300=
NM_000196.3:c.900C>A NP_000187.3:p.Ile300=
NM_000196.4:c.900C>A MANE Select NP_000187.3:p.Ile300=