Canonical Allele Identifier: CA15907462
Gene: NOS2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2274894

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27772145T>G , CM000679.2:g.27772145T>G GRCh38
NC_000017.10:g.26099171T>G , CM000679.1:g.26099171T>G GRCh37
NC_000017.9:g.23123298T>G NCBI36
NG_011470.1:g.33385A>C

Transcript Alleles

HGVS Amino-acid change
NM_000625.4:c.1704+163A>C VV NP_000616.3:p.=
XM_011524859.1:c.1704+163A>C XP_011523161.1:p.=
XM_011524860.1:c.1701+163A>C XP_011523162.1:p.=
XM_011524861.1:c.1704+163A>C XP_011523163.1:p.=
XM_011524862.1:c.1038+163A>C XP_011523164.1:p.=
ENST00000313735.10:c.1704+163A>C ENSP00000327251.6:p.=
ENST00000621962.1:n.1587+163A>C ENSP00000482291.1:p.=