Canonical Allele Identifier: CA398316639
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1909648808
MyVariant Identifiers: chr17:g.26131153G>A (hg19) chr17:g.27804127G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804127G>A , CM000679.2:g.27804127G>A GRCh38
NC_000017.10:g.26131153G>A , CM000679.1:g.26131153G>A GRCh37
NC_000017.9:g.23155280G>A NCBI36
NG_011470.1:g.1403C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.434C>T ENSP00000462879.1:p.Thr145Ile
XM_011524859.1:c.-78C>T XP_011523161.1:n.-78C>T
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