Canonical Allele Identifier: CA289078668
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1052518661
gnomAD v3: 17-27804225-G-T
gnomAD v4: 17-27804225-G-T
MyVariant Identifiers: chr17:g.26131251G>T (hg19) chr17:g.27804225G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804225G>T , CM000679.2:g.27804225G>T GRCh38
NC_000017.10:g.26131251G>T , CM000679.1:g.26131251G>T GRCh37
NC_000017.9:g.23155378G>T NCBI36
NG_011470.1:g.1305C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.336C>A ENSP00000462879.1:p.Leu112=
XM_011524859.1:c.-176C>A XP_011523161.1:n.-176C>A
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