Canonical Allele Identifier: CA2636791122
Gene: NOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804119T>A , CM000679.2:g.27804119T>A GRCh38
NC_000017.10:g.26131145T>A , CM000679.1:g.26131145T>A GRCh37
NC_000017.9:g.23155272T>A NCBI36
NG_011470.1:g.1411A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.438+4A>T ENSP00000462879.1:n.438+4A>T
XM_011524859.1:c.-74+4A>T XP_011523161.1:n.-74+4A>T