Canonical Allele Identifier: CA398317052
Gene: NOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26131250G>C (hg19) chr17:g.27804224G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804224G>C , CM000679.2:g.27804224G>C GRCh38
NC_000017.10:g.26131250G>C , CM000679.1:g.26131250G>C GRCh37
NC_000017.9:g.23155377G>C NCBI36
NG_011470.1:g.1306C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.337C>G ENSP00000462879.1:p.Gln113Glu
XM_011524859.1:c.-175C>G XP_011523161.1:n.-175C>G
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