Canonical Allele Identifier: CA2254009805
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27772187T= , CM000679.2:g.27772187T= GRCh38
NC_000017.10:g.26099213T= , CM000679.1:g.26099213T= GRCh37
NC_000017.9:g.23123340T= NCBI36
NG_011470.1:g.33343A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697337.1:c.*1271A= ENSP00000513259.1:n.*1271A=
ENST00000697338.1:c.1552+121A= ENSP00000513260.1:n.1552+121A=
ENST00000697339.1:c.738+121A= ENSP00000513261.1:n.738+121A=
ENST00000697340.1:c.*421+121A= ENSP00000513262.1:n.*421+121A=
ENST00000697341.1:n.1674+121A=
ENST00000313735.11:c.1704+121A= MANE Select ENSP00000327251.6:n.1704+121A=
ENST00000646938.1:c.1701+121A= ENSP00000494870.1:n.1701+121A=
ENST00000313735.10:c.1704+121A= ENSP00000327251.6:n.1704+121A=
ENST00000621962.1:c.1587+121A= ENSP00000482291.1:n.1587+121A=
NM_000625.4:c.1704+121A= MANE Select NP_000616.3:n.1704+121A=
XM_011524859.1:c.1704+121A= XP_011523161.1:n.1704+121A=
XM_011524860.1:c.1701+121A= XP_011523162.1:n.1701+121A=
XM_011524861.1:c.1704+121A= XP_011523163.1:n.1704+121A=
XM_011524862.1:c.1038+121A= XP_011523164.1:n.1038+121A=