Canonical Allele Identifier: CA496083070
Gene: HSD11B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67470666A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436763A>T , CM000678.2:g.67436763A>T GRCh38
NC_000016.9:g.67470666A>T , CM000678.1:g.67470666A>T GRCh37
NC_000016.8:g.66028167A>T NCBI36
NG_011482.1:g.49424T>A
NG_016549.1:g.10631A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.978A>T MANE Select ENSP00000316786.5:p.Thr326=
ENST00000326152.5:c.978A>T ENSP00000316786.5:p.Thr326=
NM_000196.3:c.978A>T NP_000187.3:p.Thr326=
NM_000196.4:c.978A>T MANE Select NP_000187.3:p.Thr326=
Search 100 bp 5'
Search 100 bp 3'