Canonical Allele Identifier: CA498791806
Gene: NOS2 HGNC NCBI

Linked Data

gnomAD v4: 17-27804317-T-G
MyVariant Identifiers: chr17:g.26131343T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804317T>G , CM000679.2:g.27804317T>G GRCh38
NC_000017.10:g.26131343T>G , CM000679.1:g.26131343T>G GRCh37
NC_000017.9:g.23155470T>G NCBI36
NG_011470.1:g.1213A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.244A>C ENSP00000462879.1:p.Arg82=
XM_011524859.1:c.-268A>C XP_011523161.1:n.-268A>C
Search 100 bp 5'
Search 100 bp 3'