Canonical Allele Identifier: CA2254020831
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1909391677
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27797561C>G , CM000679.2:g.27797561C>G GRCh38
NC_000017.10:g.26124587C>G , CM000679.1:g.26124587C>G GRCh37
NC_000017.9:g.23148714C>G NCBI36
NG_011470.1:g.7969G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000697337.1:c.110+1139G>C ENSP00000513259.1:n.110+1139G>C
ENST00000313735.11:c.110+1139G>C MANE Select ENSP00000327251.6:n.110+1139G>C
ENST00000313735.10:c.110+1139G>C ENSP00000327251.6:n.110+1139G>C
ENST00000621962.1:c.110+1139G>C ENSP00000482291.1:n.110+1139G>C
NM_000625.4:c.110+1139G>C MANE Select NP_000616.3:n.110+1139G>C
XM_011524859.1:c.110+1139G>C XP_011523161.1:n.110+1139G>C
XM_011524861.1:c.110+1139G>C XP_011523163.1:n.110+1139G>C
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