Canonical Allele Identifier: CA396278982
Gene: HSD11B2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436007G>C , CM000678.2:g.67436007G>C GRCh38
NC_000016.9:g.67469910G>C , CM000678.1:g.67469910G>C GRCh37
NC_000016.8:g.66027411G>C NCBI36
NG_016549.1:g.9875G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.529G>C MANE Select ENSP00000316786.5:p.Ala177Pro
ENST00000326152.5:c.529G>C ENSP00000316786.5:p.Ala177Pro
ENST00000566606.1:c.507G>C ENSP00000473429.1:n.507G>C
ENST00000567684.2:n.392G>C
NM_000196.3:c.529G>C NP_000187.3:p.Ala177Pro
NM_000196.4:c.529G>C MANE Select NP_000187.3:p.Ala177Pro