Canonical Allele Identifier: CA8110774
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs781423768

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436697T>C , CM000678.2:g.67436697T>C GRCh38
NC_000016.9:g.67470600T>C , CM000678.1:g.67470600T>C GRCh37
NC_000016.8:g.66028101T>C NCBI36
NG_011482.1:g.49490A>G
NG_016549.1:g.10565T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.912T>C MANE Select ENSP00000316786.5:p.His304=
ENST00000326152.5:c.912T>C ENSP00000316786.5:p.His304=
NM_000196.3:c.912T>C NP_000187.3:p.His304=
NM_000196.4:c.912T>C MANE Select NP_000187.3:p.His304=