Canonical Allele Identifier: CA289077540
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs915444049
gnomAD v2: 17-26128531-A-T
gnomAD v3: 17-27801505-A-T
gnomAD v4: 17-27801505-A-T
MyVariant Identifiers: chr17:g.26128531A>T (hg19) chr17:g.27801505A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801505A>T , CM000679.2:g.27801505A>T GRCh38
NC_000017.10:g.26128531A>T , CM000679.1:g.26128531A>T GRCh37
NC_000017.9:g.23152658A>T NCBI36
NG_011470.1:g.4025T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.438+2618T>A ENSP00000462879.1:n.438+2618T>A
XM_011524859.1:c.-74+2618T>A XP_011523161.1:n.-74+2618T>A
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