Canonical Allele Identifier: CA289077571
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs991444418
gnomAD v3: 17-27801602-T-G
gnomAD v4: 17-27801602-T-G
MyVariant Identifiers: chr17:g.26128628T>G (hg19) chr17:g.27801602T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801602T>G , CM000679.2:g.27801602T>G GRCh38
NC_000017.10:g.26128628T>G , CM000679.1:g.26128628T>G GRCh37
NC_000017.9:g.23152755T>G NCBI36
NG_011470.1:g.3928A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.438+2521A>C ENSP00000462879.1:n.438+2521A>C
XM_011524859.1:c.-74+2521A>C XP_011523161.1:n.-74+2521A>C
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