Canonical Allele Identifier: CA2254008349
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27769504G= , CM000679.2:g.27769504G= GRCh38
NC_000017.10:g.26096530G= , CM000679.1:g.26096530G= GRCh37
NC_000017.9:g.23120657G= NCBI36
NG_011470.1:g.36026C=

Transcript Alleles

HGVS Amino-acid change
ENST00000697337.1:c.*2595+31C= ENSP00000513259.1:n.*2595+31C=
ENST00000697338.1:c.1707+31C= ENSP00000513260.1:n.1707+31C=
ENST00000697339.1:c.893+31C= ENSP00000513261.1:n.893+31C=
ENST00000697340.1:c.*576+31C= ENSP00000513262.1:n.*576+31C=
ENST00000697341.1:n.1829+31C=
ENST00000313735.11:c.1859+31C= MANE Select ENSP00000327251.6:n.1859+31C=
ENST00000646938.1:c.1856+31C= ENSP00000494870.1:n.1856+31C=
ENST00000313735.10:c.1859+31C= ENSP00000327251.6:n.1859+31C=
ENST00000621962.1:c.1742+31C= ENSP00000482291.1:n.1742+31C=
NM_000625.4:c.1859+31C= MANE Select NP_000616.3:n.1859+31C=
XM_011524859.1:c.1859+31C= XP_011523161.1:n.1859+31C=
XM_011524860.1:c.1856+31C= XP_011523162.1:n.1856+31C=
XM_011524861.1:c.1859+31C= XP_011523163.1:n.1859+31C=
XM_011524862.1:c.1193+31C= XP_011523164.1:n.1193+31C=