Canonical Allele Identifier: CA396282628
Gene: HSD11B2 HGNC NCBI

Linked Data

gnomAD v4: 16-67436752-G-T
MyVariant Identifiers: chr16:g.67470655G>T (hg19) chr16:g.67436752G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436752G>T , CM000678.2:g.67436752G>T GRCh38
NC_000016.9:g.67470655G>T , CM000678.1:g.67470655G>T GRCh37
NC_000016.8:g.66028156G>T NCBI36
NG_011482.1:g.49435C>A
NG_016549.1:g.10620G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.967G>T MANE Select ENSP00000316786.5:p.Asp323Tyr
ENST00000326152.5:c.967G>T ENSP00000316786.5:p.Asp323Tyr
NM_000196.3:c.967G>T NP_000187.3:p.Asp323Tyr
NM_000196.4:c.967G>T MANE Select NP_000187.3:p.Asp323Tyr
Search 100 bp 5'
Search 100 bp 3'