Canonical Allele Identifier: CA398317409
Gene: NOS2 HGNC NCBI

Linked Data

gnomAD v4: 17-27804322-A-G
MyVariant Identifiers: chr17:g.26131348A>G (hg19) chr17:g.27804322A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804322A>G , CM000679.2:g.27804322A>G GRCh38
NC_000017.10:g.26131348A>G , CM000679.1:g.26131348A>G GRCh37
NC_000017.9:g.23155475A>G NCBI36
NG_011470.1:g.1208T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.239T>C ENSP00000462879.1:p.Ile80Thr
XM_011524859.1:c.-273T>C XP_011523161.1:n.-273T>C
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