Canonical Allele Identifier: CA398301534

Gene: NOS2

Linked Data

• gnomAD v4: 17-27769571-G-C
• MyVariant Identifiers: chr17:g.26096597G>C (hg19) ; chr17:g.27769571G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27769571G>C , CM000679.2:g.27769571G>C	GRCh38
NC_000017.10:g.26096597G>C , CM000679.1:g.26096597G>C	GRCh37
NC_000017.9:g.23120724G>C	NCBI36
NG_011470.1:g.35959C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*2559C>G	ENSP00000513259.1:n.*2559C>G
ENST00000697338.1:c.1671C>G	ENSP00000513260.1:n.1671C>G
ENST00000697339.1:c.857C>G	ENSP00000513261.1:p.Ser286Trp
ENST00000697340.1:c.*540C>G	ENSP00000513262.1:n.*540C>G
ENST00000697341.1:n.1793C>G
ENST00000313735.11:c.1823C>G MANE Select	ENSP00000327251.6:p.Ser608Trp
ENST00000646938.1:c.1820C>G	ENSP00000494870.1:p.Ser607Trp
ENST00000313735.10:c.1823C>G	ENSP00000327251.6:p.Ser608Trp
ENST00000621962.1:c.1706C>G	ENSP00000482291.1:p.Ser569Trp
NM_000625.4:c.1823C>G MANE Select	NP_000616.3:p.Ser608Trp
XM_011524859.1:c.1823C>G	XP_011523161.1:p.Ser608Trp
XM_011524860.1:c.1820C>G	XP_011523162.1:p.Ser607Trp
XM_011524861.1:c.1823C>G	XP_011523163.1:p.Ser608Trp
XM_011524862.1:c.1157C>G	XP_011523164.1:p.Ser386Trp