Canonical Allele Identifier: CA289075429
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs34921306
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27797656dup , CM000679.2:g.27797656dup GRCh38
NC_000017.10:g.26124682dup , CM000679.1:g.26124682dup GRCh37
NC_000017.9:g.23148809dup NCBI36
NG_011470.1:g.7874dup

Transcript Alleles

HGVS Amino-acid change
ENST00000697337.1:c.110+1044dup ENSP00000513259.1:n.110+1044dup
ENST00000313735.11:c.110+1044dup MANE Select ENSP00000327251.6:n.110+1044dup
ENST00000313735.10:c.110+1044dup ENSP00000327251.6:n.110+1044dup
ENST00000621962.1:c.110+1044dup ENSP00000482291.1:n.110+1044dup
NM_000625.4:c.110+1044dup MANE Select NP_000616.3:n.110+1044dup
XM_011524859.1:c.110+1044dup XP_011523161.1:n.110+1044dup
XM_011524861.1:c.110+1044dup XP_011523163.1:n.110+1044dup
Search 100 bp 5'
Search 100 bp 3'