Canonical Allele Identifier: CA398316631
Gene: NOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26131151A>T (hg19) chr17:g.27804125A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804125A>T , CM000679.2:g.27804125A>T GRCh38
NC_000017.10:g.26131151A>T , CM000679.1:g.26131151A>T GRCh37
NC_000017.9:g.23155278A>T NCBI36
NG_011470.1:g.1405T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.436T>A ENSP00000462879.1:p.Leu146Met
XM_011524859.1:c.-76T>A XP_011523161.1:n.-76T>A
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