Canonical Allele Identifier: CA289078674
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs535087199
gnomAD v2: 17-26131271-G-A
gnomAD v3: 17-27804245-G-A
gnomAD v4: 17-27804245-G-A
MyVariant Identifiers: chr17:g.26131271G>A (hg19) chr17:g.27804245G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804245G>A , CM000679.2:g.27804245G>A GRCh38
NC_000017.10:g.26131271G>A , CM000679.1:g.26131271G>A GRCh37
NC_000017.9:g.23155398G>A NCBI36
NG_011470.1:g.1285C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.316C>T ENSP00000462879.1:p.Arg106Cys
XM_011524859.1:c.-196C>T XP_011523161.1:n.-196C>T
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