Canonical Allele Identifier: CA396282051
Gene: HSD11B2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67470583T>G (hg19) chr16:g.67436680T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436680T>G , CM000678.2:g.67436680T>G GRCh38
NC_000016.9:g.67470583T>G , CM000678.1:g.67470583T>G GRCh37
NC_000016.8:g.66028084T>G NCBI36
NG_011482.1:g.49507A>C
NG_016549.1:g.10548T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.895T>G MANE Select ENSP00000316786.5:p.Tyr299Asp
ENST00000326152.5:c.895T>G ENSP00000316786.5:p.Tyr299Asp
NM_000196.3:c.895T>G NP_000187.3:p.Tyr299Asp
NM_000196.4:c.895T>G MANE Select NP_000187.3:p.Tyr299Asp
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