Canonical Allele Identifier: CA727658926
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1337702891
gnomAD v3: 17-27797559-C-T
gnomAD v4: 17-27797559-C-T
MyVariant Identifiers: chr17:g.26124585C>T (hg19) chr17:g.27797559C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27797559C>T , CM000679.2:g.27797559C>T GRCh38
NC_000017.10:g.26124585C>T , CM000679.1:g.26124585C>T GRCh37
NC_000017.9:g.23148712C>T NCBI36
NG_011470.1:g.7971G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000697337.1:c.110+1141G>A ENSP00000513259.1:n.110+1141G>A
ENST00000313735.11:c.110+1141G>A MANE Select ENSP00000327251.6:n.110+1141G>A
ENST00000313735.10:c.110+1141G>A ENSP00000327251.6:n.110+1141G>A
ENST00000621962.1:c.110+1141G>A ENSP00000482291.1:n.110+1141G>A
NM_000625.4:c.110+1141G>A MANE Select NP_000616.3:n.110+1141G>A
XM_011524859.1:c.110+1141G>A XP_011523161.1:n.110+1141G>A
XM_011524861.1:c.110+1141G>A XP_011523163.1:n.110+1141G>A
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