Canonical Allele Identifier: CA398317056
Gene: NOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26131252A>C (hg19) chr17:g.27804226A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804226A>C , CM000679.2:g.27804226A>C GRCh38
NC_000017.10:g.26131252A>C , CM000679.1:g.26131252A>C GRCh37
NC_000017.9:g.23155379A>C NCBI36
NG_011470.1:g.1304T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.335T>G ENSP00000462879.1:p.Leu112Arg
XM_011524859.1:c.-177T>G XP_011523161.1:n.-177T>G
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