Canonical Allele Identifier: CA496082679
Gene: HSD11B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67469975G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436072G>A , CM000678.2:g.67436072G>A GRCh38
NC_000016.9:g.67469975G>A , CM000678.1:g.67469975G>A GRCh37
NC_000016.8:g.66027476G>A NCBI36
NG_011482.1:g.50115C>T
NG_016549.1:g.9940G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.594G>A MANE Select ENSP00000316786.5:p.Glu198=
ENST00000326152.5:c.594G>A ENSP00000316786.5:p.Glu198=
ENST00000566606.1:c.572G>A ENSP00000473429.1:n.572G>A
ENST00000567684.2:n.457G>A
NM_000196.3:c.594G>A NP_000187.3:p.Glu198=
NM_000196.4:c.594G>A MANE Select NP_000187.3:p.Glu198=