Canonical Allele Identifier: CA498791891
Gene: NOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26131350G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804324G>C , CM000679.2:g.27804324G>C GRCh38
NC_000017.10:g.26131350G>C , CM000679.1:g.26131350G>C GRCh37
NC_000017.9:g.23155477G>C NCBI36
NG_011470.1:g.1206C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.237C>G ENSP00000462879.1:p.Ser79=
XM_011524859.1:c.-275C>G XP_011523161.1:n.-275C>G
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