Canonical Allele Identifier: CA498791812
Gene: NOS2 HGNC NCBI

Linked Data

gnomAD v4: 17-27804318-G-T
MyVariant Identifiers: chr17:g.26131344G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804318G>T , CM000679.2:g.27804318G>T GRCh38
NC_000017.10:g.26131344G>T , CM000679.1:g.26131344G>T GRCh37
NC_000017.9:g.23155471G>T NCBI36
NG_011470.1:g.1212C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.243C>A ENSP00000462879.1:p.Ile81=
XM_011524859.1:c.-269C>A XP_011523161.1:n.-269C>A
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