Canonical Allele Identifier: CA289078616
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs761326756
gnomAD v2: 17-26131142-G-A
gnomAD v3: 17-27804116-G-A
gnomAD v4: 17-27804116-G-A
MyVariant Identifiers: chr17:g.26131142G>A (hg19) chr17:g.27804116G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804116G>A , CM000679.2:g.27804116G>A GRCh38
NC_000017.10:g.26131142G>A , CM000679.1:g.26131142G>A GRCh37
NC_000017.9:g.23155269G>A NCBI36
NG_011470.1:g.1414C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.438+7C>T ENSP00000462879.1:n.438+7C>T
XM_011524859.1:c.-74+7C>T XP_011523161.1:n.-74+7C>T
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