Canonical Allele Identifier: CA2229310354
Gene: HSD11B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436584C= , CM000678.2:g.67436584C= GRCh38
NC_000016.9:g.67470487C= , CM000678.1:g.67470487C= GRCh37
NC_000016.8:g.66027988C= NCBI36
NG_011482.1:g.49603G=
NG_016549.1:g.10452C=

Transcript Alleles

HGVS Amino-acid change
ENST00000326152.6:c.803-4C= MANE Select ENSP00000316786.5:n.803-4C=
ENST00000326152.5:c.803-4C= ENSP00000316786.5:n.803-4C=
NM_000196.3:c.803-4C= NP_000187.3:n.803-4C=
NM_000196.4:c.803-4C= MANE Select NP_000187.3:n.803-4C=