Canonical Allele Identifier: CA2576205153
Gene: NOS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27769479C>T , CM000679.2:g.27769479C>T GRCh38
NC_000017.10:g.26096505C>T , CM000679.1:g.26096505C>T GRCh37
NC_000017.9:g.23120632C>T NCBI36
NG_011470.1:g.36051G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000697337.1:c.*2595+56G>A ENSP00000513259.1:n.*2595+56G>A
ENST00000697338.1:c.1707+56G>A ENSP00000513260.1:n.1707+56G>A
ENST00000697339.1:c.893+56G>A ENSP00000513261.1:n.893+56G>A
ENST00000697340.1:c.*576+56G>A ENSP00000513262.1:n.*576+56G>A
ENST00000697341.1:n.1829+56G>A
ENST00000313735.11:c.1859+56G>A MANE Select ENSP00000327251.6:n.1859+56G>A
ENST00000646938.1:c.1856+56G>A ENSP00000494870.1:n.1856+56G>A
ENST00000313735.10:c.1859+56G>A ENSP00000327251.6:n.1859+56G>A
ENST00000621962.1:c.1742+56G>A ENSP00000482291.1:n.1742+56G>A
NM_000625.4:c.1859+56G>A MANE Select NP_000616.3:n.1859+56G>A
XM_011524859.1:c.1859+56G>A XP_011523161.1:n.1859+56G>A
XM_011524860.1:c.1856+56G>A XP_011523162.1:n.1856+56G>A
XM_011524861.1:c.1859+56G>A XP_011523163.1:n.1859+56G>A
XM_011524862.1:c.1193+56G>A XP_011523164.1:n.1193+56G>A
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