Canonical Allele Identifier: CA982708880
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1210726064
gnomAD v3: 17-27801481-G-T
gnomAD v4: 17-27801481-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801481G>T , CM000679.2:g.27801481G>T GRCh38
NC_000017.10:g.26128507G>T , CM000679.1:g.26128507G>T GRCh37
NC_000017.9:g.23152634G>T NCBI36
NG_011470.1:g.4049C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.439-2599C>A ENSP00000462879.1:n.439-2599C>A
XM_011524859.1:c.-73-2599C>A XP_011523161.1:n.-73-2599C>A
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