Canonical Allele Identifier: CA398316656
Gene: NOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26131157C>T (hg19) chr17:g.27804131C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804131C>T , CM000679.2:g.27804131C>T GRCh38
NC_000017.10:g.26131157C>T , CM000679.1:g.26131157C>T GRCh37
NC_000017.9:g.23155284C>T NCBI36
NG_011470.1:g.1399G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.430G>A ENSP00000462879.1:p.Val144Met
XM_011524859.1:c.-82G>A XP_011523161.1:n.-82G>A
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