Canonical Allele Identifier: CA289063718
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs769551855

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27783827G>A , CM000679.2:g.27783827G>A GRCh38
NC_000017.10:g.26110853G>A , CM000679.1:g.26110853G>A GRCh37
NC_000017.9:g.23134980G>A NCBI36
NG_011470.1:g.21703C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000697337.1:c.319-721C>T ENSP00000513259.1:n.319-721C>T
ENST00000697338.1:c.316-721C>T ENSP00000513260.1:n.316-721C>T
ENST00000697339.1:c.315+4982C>T ENSP00000513261.1:n.315+4982C>T
ENST00000697340.1:c.465-721C>T ENSP00000513262.1:n.465-721C>T
ENST00000697341.1:n.438-721C>T
ENST00000313735.11:c.468-721C>T MANE Select ENSP00000327251.6:n.468-721C>T
ENST00000646938.1:c.465-721C>T ENSP00000494870.1:n.465-721C>T
ENST00000313735.10:c.468-721C>T ENSP00000327251.6:n.468-721C>T
ENST00000621962.1:c.468-721C>T ENSP00000482291.1:n.468-721C>T
NM_000625.4:c.468-721C>T MANE Select NP_000616.3:n.468-721C>T
XM_011524859.1:c.468-721C>T XP_011523161.1:n.468-721C>T
XM_011524860.1:c.465-721C>T XP_011523162.1:n.465-721C>T
XM_011524861.1:c.468-721C>T XP_011523163.1:n.468-721C>T
XM_011524862.1:c.-199-721C>T XP_011523164.1:n.-199-721C>T