Canonical Allele Identifier: CA498790035
Gene: NOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26131158A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804132A>G , CM000679.2:g.27804132A>G GRCh38
NC_000017.10:g.26131158A>G , CM000679.1:g.26131158A>G GRCh37
NC_000017.9:g.23155285A>G NCBI36
NG_011470.1:g.1398T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.429T>C ENSP00000462879.1:p.Cys143=
XM_011524859.1:c.-83T>C XP_011523161.1:n.-83T>C
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