Canonical Allele Identifier: CA396282065
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs2040977070
gnomAD v3: 16-67436681-A-G
gnomAD v4: 16-67436681-A-G
MyVariant Identifiers: chr16:g.67470584A>G (hg19) chr16:g.67436681A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436681A>G , CM000678.2:g.67436681A>G GRCh38
NC_000016.9:g.67470584A>G , CM000678.1:g.67470584A>G GRCh37
NC_000016.8:g.66028085A>G NCBI36
NG_011482.1:g.49506T>C
NG_016549.1:g.10549A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.896A>G MANE Select ENSP00000316786.5:p.Tyr299Cys
ENST00000326152.5:c.896A>G ENSP00000316786.5:p.Tyr299Cys
NM_000196.3:c.896A>G NP_000187.3:p.Tyr299Cys
NM_000196.4:c.896A>G MANE Select NP_000187.3:p.Tyr299Cys
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