Canonical Allele Identifier: CA2254020811
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1909388745
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27797518T>C , CM000679.2:g.27797518T>C GRCh38
NC_000017.10:g.26124544T>C , CM000679.1:g.26124544T>C GRCh37
NC_000017.9:g.23148671T>C NCBI36
NG_011470.1:g.8012A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000697337.1:c.110+1182A>G ENSP00000513259.1:n.110+1182A>G
ENST00000313735.11:c.110+1182A>G MANE Select ENSP00000327251.6:n.110+1182A>G
ENST00000313735.10:c.110+1182A>G ENSP00000327251.6:n.110+1182A>G
ENST00000621962.1:c.110+1182A>G ENSP00000482291.1:n.110+1182A>G
NM_000625.4:c.110+1182A>G MANE Select NP_000616.3:n.110+1182A>G
XM_011524859.1:c.110+1182A>G XP_011523161.1:n.110+1182A>G
XM_011524861.1:c.110+1182A>G XP_011523163.1:n.110+1182A>G
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