Canonical Allele Identifier: CA398317021
Gene: NOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26131243C>G (hg19) chr17:g.27804217C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804217C>G , CM000679.2:g.27804217C>G GRCh38
NC_000017.10:g.26131243C>G , CM000679.1:g.26131243C>G GRCh37
NC_000017.9:g.23155370C>G NCBI36
NG_011470.1:g.1313G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.344G>C ENSP00000462879.1:p.Gly115Ala
XM_011524859.1:c.-168G>C XP_011523161.1:n.-168G>C
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