Canonical Allele Identifier: CA496082735
Gene: HSD11B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67470017C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436114C>A , CM000678.2:g.67436114C>A GRCh38
NC_000016.9:g.67470017C>A , CM000678.1:g.67470017C>A GRCh37
NC_000016.8:g.66027518C>A NCBI36
NG_011482.1:g.50073G>T
NG_016549.1:g.9982C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000326152.6:c.636C>A MANE Select ENSP00000316786.5:p.Gly212=
ENST00000326152.5:c.636C>A ENSP00000316786.5:p.Gly212=
ENST00000566606.1:c.614C>A ENSP00000473429.1:n.614C>A
ENST00000567684.2:n.499C>A
NM_000196.3:c.636C>A NP_000187.3:p.Gly212=
NM_000196.4:c.636C>A MANE Select NP_000187.3:p.Gly212=
Search 100 bp 5'
Search 100 bp 3'