Canonical Allele Identifier: CA289077584
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs973607276
gnomAD v3: 17-27801658-G-T
gnomAD v4: 17-27801658-G-T
MyVariant Identifiers: chr17:g.26128684G>T (hg19) chr17:g.27801658G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801658G>T , CM000679.2:g.27801658G>T GRCh38
NC_000017.10:g.26128684G>T , CM000679.1:g.26128684G>T GRCh37
NC_000017.9:g.23152811G>T NCBI36
NG_011470.1:g.3872C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.438+2465C>A ENSP00000462879.1:n.438+2465C>A
XM_011524859.1:c.-74+2465C>A XP_011523161.1:n.-74+2465C>A
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