Canonical Allele Identifier: CA498789951
Gene: NOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26131152G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804126G>C , CM000679.2:g.27804126G>C GRCh38
NC_000017.10:g.26131152G>C , CM000679.1:g.26131152G>C GRCh37
NC_000017.9:g.23155279G>C NCBI36
NG_011470.1:g.1404C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.435C>G ENSP00000462879.1:p.Thr145=
XM_011524859.1:c.-77C>G XP_011523161.1:n.-77C>G
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