Canonical Allele Identifier: CA289078612
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs577291756
gnomAD v3: 17-27804100-T-C
gnomAD v4: 17-27804100-T-C
COSMIC: COSN16321882
MyVariant Identifiers: chr17:g.26131126T>C (hg19) chr17:g.27804100T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804100T>C , CM000679.2:g.27804100T>C GRCh38
NC_000017.10:g.26131126T>C , CM000679.1:g.26131126T>C GRCh37
NC_000017.9:g.23155253T>C NCBI36
NG_011470.1:g.1430A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.438+23A>G ENSP00000462879.1:n.438+23A>G
XM_011524859.1:c.-74+23A>G XP_011523161.1:n.-74+23A>G
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