Canonical Allele Identifier: CA2254020822
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1028716125
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27797544C>A , CM000679.2:g.27797544C>A GRCh38
NC_000017.10:g.26124570C>A , CM000679.1:g.26124570C>A GRCh37
NC_000017.9:g.23148697C>A NCBI36
NG_011470.1:g.7986G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000697337.1:c.110+1156G>T ENSP00000513259.1:n.110+1156G>T
ENST00000313735.11:c.110+1156G>T MANE Select ENSP00000327251.6:n.110+1156G>T
ENST00000313735.10:c.110+1156G>T ENSP00000327251.6:n.110+1156G>T
ENST00000621962.1:c.110+1156G>T ENSP00000482291.1:n.110+1156G>T
NM_000625.4:c.110+1156G>T MANE Select NP_000616.3:n.110+1156G>T
XM_011524859.1:c.110+1156G>T XP_011523161.1:n.110+1156G>T
XM_011524861.1:c.110+1156G>T XP_011523163.1:n.110+1156G>T
Search 100 bp 5'
Search 100 bp 3'