Canonical Allele Identifier: CA498791042
Gene: NOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26131263T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804237T>C , CM000679.2:g.27804237T>C GRCh38
NC_000017.10:g.26131263T>C , CM000679.1:g.26131263T>C GRCh37
NC_000017.9:g.23155390T>C NCBI36
NG_011470.1:g.1293A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.324A>G ENSP00000462879.1:p.Arg108=
XM_011524859.1:c.-188A>G XP_011523161.1:n.-188A>G
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