Canonical Allele Identifier: CA496082756
Gene: HSD11B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67470029T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436126T>C , CM000678.2:g.67436126T>C GRCh38
NC_000016.9:g.67470029T>C , CM000678.1:g.67470029T>C GRCh37
NC_000016.8:g.66027530T>C NCBI36
NG_011482.1:g.50061A>G
NG_016549.1:g.9994T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.648T>C MANE Select ENSP00000316786.5:p.Thr216=
ENST00000326152.5:c.648T>C ENSP00000316786.5:p.Thr216=
ENST00000566606.1:c.626T>C ENSP00000473429.1:n.626T>C
ENST00000567684.2:n.511T>C
NM_000196.3:c.648T>C NP_000187.3:p.Thr216=
NM_000196.4:c.648T>C MANE Select NP_000187.3:p.Thr216=
Search 100 bp 5'
Search 100 bp 3'