Canonical Allele Identifier: CA2254020805
Gene: NOS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27797506T= , CM000679.2:g.27797506T= GRCh38
NC_000017.10:g.26124532T= , CM000679.1:g.26124532T= GRCh37
NC_000017.9:g.23148659T= NCBI36
NG_011470.1:g.8024A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697337.1:c.110+1194A= ENSP00000513259.1:n.110+1194A=
ENST00000313735.11:c.110+1194A= MANE Select ENSP00000327251.6:n.110+1194A=
ENST00000313735.10:c.110+1194A= ENSP00000327251.6:n.110+1194A=
ENST00000621962.1:c.110+1194A= ENSP00000482291.1:n.110+1194A=
NM_000625.4:c.110+1194A= MANE Select NP_000616.3:n.110+1194A=
XM_011524859.1:c.110+1194A= XP_011523161.1:n.110+1194A=
XM_011524861.1:c.110+1194A= XP_011523163.1:n.110+1194A=
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