Canonical Allele Identifier: CA498789939
Gene: NOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26131151A>G (hg19)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.436T>C ENSP00000462879.1:p.Leu146=
XM_011524859.1:c.-76T>C XP_011523161.1:n.-76T>C
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