Canonical Allele Identifier: CA289063739
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs749086428

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27783864C>T , CM000679.2:g.27783864C>T GRCh38
NC_000017.10:g.26110890C>T , CM000679.1:g.26110890C>T GRCh37
NC_000017.9:g.23135017C>T NCBI36
NG_011470.1:g.21666G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000697337.1:c.319-758G>A ENSP00000513259.1:n.319-758G>A
ENST00000697338.1:c.316-758G>A ENSP00000513260.1:n.316-758G>A
ENST00000697339.1:c.315+4945G>A ENSP00000513261.1:n.315+4945G>A
ENST00000697340.1:c.465-758G>A ENSP00000513262.1:n.465-758G>A
ENST00000697341.1:n.438-758G>A
ENST00000313735.11:c.468-758G>A MANE Select ENSP00000327251.6:n.468-758G>A
ENST00000646938.1:c.465-758G>A ENSP00000494870.1:n.465-758G>A
ENST00000313735.10:c.468-758G>A ENSP00000327251.6:n.468-758G>A
ENST00000621962.1:c.468-758G>A ENSP00000482291.1:n.468-758G>A
NM_000625.4:c.468-758G>A MANE Select NP_000616.3:n.468-758G>A
XM_011524859.1:c.468-758G>A XP_011523161.1:n.468-758G>A
XM_011524860.1:c.465-758G>A XP_011523162.1:n.465-758G>A
XM_011524861.1:c.468-758G>A XP_011523163.1:n.468-758G>A
XM_011524862.1:c.-199-758G>A XP_011523164.1:n.-199-758G>A