Canonical Allele Identifier: CA727661043
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1207402296
gnomAD v3: 17-27801413-A-T
gnomAD v4: 17-27801413-A-T
MyVariant Identifiers: chr17:g.26128439A>T (hg19) chr17:g.27801413A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801413A>T , CM000679.2:g.27801413A>T GRCh38
NC_000017.10:g.26128439A>T , CM000679.1:g.26128439A>T GRCh37
NC_000017.9:g.23152566A>T NCBI36
NG_011470.1:g.4117T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.439-2531T>A ENSP00000462879.1:n.439-2531T>A
XM_011524859.1:c.-73-2531T>A XP_011523161.1:n.-73-2531T>A
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