Canonical Allele Identifier: CA396279063
Gene: HSD11B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67469923C>A (hg19) chr16:g.67436020C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436020C>A , CM000678.2:g.67436020C>A GRCh38
NC_000016.9:g.67469923C>A , CM000678.1:g.67469923C>A GRCh37
NC_000016.8:g.66027424C>A NCBI36
NG_011482.1:g.50167G>T
NG_016549.1:g.9888C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.542C>A MANE Select ENSP00000316786.5:p.Pro181Gln
ENST00000326152.5:c.542C>A ENSP00000316786.5:p.Pro181Gln
ENST00000566606.1:c.520C>A ENSP00000473429.1:n.520C>A
ENST00000567684.2:n.405C>A
NM_000196.3:c.542C>A NP_000187.3:p.Pro181Gln
NM_000196.4:c.542C>A MANE Select NP_000187.3:p.Pro181Gln
Search 100 bp 5'
Search 100 bp 3'