Canonical Allele Identifier: CA982708872
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1909547809
gnomAD v3: 17-27801438-G-C
gnomAD v4: 17-27801438-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27801438G>C , CM000679.2:g.27801438G>C GRCh38
NC_000017.10:g.26128464G>C , CM000679.1:g.26128464G>C GRCh37
NC_000017.9:g.23152591G>C NCBI36
NG_011470.1:g.4092C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.439-2556C>G ENSP00000462879.1:n.439-2556C>G
XM_011524859.1:c.-73-2556C>G XP_011523161.1:n.-73-2556C>G
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