Canonical Allele Identifier: CA289078615
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs776061331
gnomAD v2: 17-26131140-G-C
gnomAD v3: 17-27804114-G-C
gnomAD v4: 17-27804114-G-C
MyVariant Identifiers: chr17:g.26131140G>C (hg19) chr17:g.27804114G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804114G>C , CM000679.2:g.27804114G>C GRCh38
NC_000017.10:g.26131140G>C , CM000679.1:g.26131140G>C GRCh37
NC_000017.9:g.23155267G>C NCBI36
NG_011470.1:g.1416C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.438+9C>G ENSP00000462879.1:n.438+9C>G
XM_011524859.1:c.-74+9C>G XP_011523161.1:n.-74+9C>G
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