Canonical Allele Identifier: CA289077447
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1056785448
MyVariant Identifiers: chr17:g.26128403C>A (hg19) chr17:g.27801377C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801377C>A , CM000679.2:g.27801377C>A GRCh38
NC_000017.10:g.26128403C>A , CM000679.1:g.26128403C>A GRCh37
NC_000017.9:g.23152530C>A NCBI36
NG_011470.1:g.4153G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.439-2495G>T ENSP00000462879.1:n.439-2495G>T
XM_011524859.1:c.-73-2495G>T XP_011523161.1:n.-73-2495G>T
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