Canonical Allele Identifier: CA496082706
Gene: HSD11B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67469996C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436093C>G , CM000678.2:g.67436093C>G GRCh38
NC_000016.9:g.67469996C>G , CM000678.1:g.67469996C>G GRCh37
NC_000016.8:g.66027497C>G NCBI36
NG_011482.1:g.50094G>C
NG_016549.1:g.9961C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.615C>G MANE Select ENSP00000316786.5:p.Pro205=
ENST00000326152.5:c.615C>G ENSP00000316786.5:p.Pro205=
ENST00000566606.1:c.593C>G ENSP00000473429.1:n.593C>G
ENST00000567684.2:n.478C>G
NM_000196.3:c.615C>G NP_000187.3:p.Pro205=
NM_000196.4:c.615C>G MANE Select NP_000187.3:p.Pro205=
Search 100 bp 5'
Search 100 bp 3'