Canonical Allele Identifier: CA496082674
Gene: HSD11B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67469972C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436069C>A , CM000678.2:g.67436069C>A GRCh38
NC_000016.9:g.67469972C>A , CM000678.1:g.67469972C>A GRCh37
NC_000016.8:g.66027473C>A NCBI36
NG_011482.1:g.50118G>T
NG_016549.1:g.9937C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.591C>A MANE Select ENSP00000316786.5:p.Leu197=
ENST00000326152.5:c.591C>A ENSP00000316786.5:p.Leu197=
ENST00000566606.1:c.569C>A ENSP00000473429.1:n.569C>A
ENST00000567684.2:n.454C>A
NM_000196.3:c.591C>A NP_000187.3:p.Leu197=
NM_000196.4:c.591C>A MANE Select NP_000187.3:p.Leu197=
Search 100 bp 5'
Search 100 bp 3'