Canonical Allele Identifier: CA396281546
Gene: HSD11B2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436587G>A , CM000678.2:g.67436587G>A GRCh38
NC_000016.9:g.67470490G>A , CM000678.1:g.67470490G>A GRCh37
NC_000016.8:g.66027991G>A NCBI36
NG_011482.1:g.49600C>T
NG_016549.1:g.10455G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000326152.6:c.803-1G>A MANE Select ENSP00000316786.5:n.803-1G>A
ENST00000326152.5:c.803-1G>A ENSP00000316786.5:n.803-1G>A
NM_000196.3:c.803-1G>A NP_000187.3:n.803-1G>A
NM_000196.4:c.803-1G>A MANE Select NP_000187.3:n.803-1G>A