Canonical Allele Identifier: CA2809098447
Gene: NOS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27797737_27797747del , CM000679.2:g.27797737_27797747del GRCh38
NC_000017.10:g.26124763_26124773del , CM000679.1:g.26124763_26124773del GRCh37
NC_000017.9:g.23148890_23148900del NCBI36
NG_011470.1:g.7786_7796del

Transcript Alleles

HGVS Amino-acid Change
ENST00000697337.1:c.110+956_110+966del ENSP00000513259.1:n.110+956_110+966del
ENST00000313735.11:c.110+956_110+966del MANE Select ENSP00000327251.6:n.110+956_110+966del
ENST00000313735.10:c.110+956_110+966del ENSP00000327251.6:n.110+956_110+966del
ENST00000621962.1:c.110+956_110+966del ENSP00000482291.1:n.110+956_110+966del
NM_000625.4:c.110+956_110+966del MANE Select NP_000616.3:n.110+956_110+966del
XM_011524859.1:c.110+956_110+966del XP_011523161.1:n.110+956_110+966del
XM_011524861.1:c.110+956_110+966del XP_011523163.1:n.110+956_110+966del
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