Canonical Allele Identifier: CA396278959
Gene: HSD11B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67469907G>A (hg19) chr16:g.67436004G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436004G>A , CM000678.2:g.67436004G>A GRCh38
NC_000016.9:g.67469907G>A , CM000678.1:g.67469907G>A GRCh37
NC_000016.8:g.66027408G>A NCBI36
NG_016549.1:g.9872G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.526G>A MANE Select ENSP00000316786.5:p.Asp176Asn
ENST00000326152.5:c.526G>A ENSP00000316786.5:p.Asp176Asn
ENST00000566606.1:c.504G>A ENSP00000473429.1:n.504G>A
ENST00000567684.2:n.389G>A
NM_000196.3:c.526G>A NP_000187.3:p.Asp176Asn
NM_000196.4:c.526G>A MANE Select NP_000187.3:p.Asp176Asn
Search 100 bp 5'
Search 100 bp 3'