Canonical Allele Identifier: CA498791924
Gene: NOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26131353T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804327T>A , CM000679.2:g.27804327T>A GRCh38
NC_000017.10:g.26131353T>A , CM000679.1:g.26131353T>A GRCh37
NC_000017.9:g.23155480T>A NCBI36
NG_011470.1:g.1203A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.234A>T ENSP00000462879.1:p.Ala78=
XM_011524859.1:c.-278A>T XP_011523161.1:n.-278A>T
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