Canonical Allele Identifier: CA498791769
Gene: NOS2 HGNC NCBI

Linked Data

gnomAD v4: 17-27804315-T-C
MyVariant Identifiers: chr17:g.26131341T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804315T>C , CM000679.2:g.27804315T>C GRCh38
NC_000017.10:g.26131341T>C , CM000679.1:g.26131341T>C GRCh37
NC_000017.9:g.23155468T>C NCBI36
NG_011470.1:g.1215A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.246A>G ENSP00000462879.1:p.Arg82=
XM_011524859.1:c.-266A>G XP_011523161.1:n.-266A>G
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