Canonical Allele Identifier: CA398301494

Gene: NOS2

Linked Data

• gnomAD v4: 17-27769562-A-G
• MyVariant Identifiers: chr17:g.26096588A>G (hg19) ; chr17:g.27769562A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27769562A>G , CM000679.2:g.27769562A>G	GRCh38
NC_000017.10:g.26096588A>G , CM000679.1:g.26096588A>G	GRCh37
NC_000017.9:g.23120715A>G	NCBI36
NG_011470.1:g.35968T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*2568T>C	ENSP00000513259.1:n.*2568T>C
ENST00000697338.1:c.1680T>C	ENSP00000513260.1:n.1680T>C
ENST00000697339.1:c.866T>C	ENSP00000513261.1:p.Met289Thr
ENST00000697340.1:c.*549T>C	ENSP00000513262.1:n.*549T>C
ENST00000697341.1:n.1802T>C
ENST00000313735.11:c.1832T>C MANE Select	ENSP00000327251.6:p.Met611Thr
ENST00000646938.1:c.1829T>C	ENSP00000494870.1:p.Met610Thr
ENST00000313735.10:c.1832T>C	ENSP00000327251.6:p.Met611Thr
ENST00000621962.1:c.1715T>C	ENSP00000482291.1:p.Met572Thr
NM_000625.4:c.1832T>C MANE Select	NP_000616.3:p.Met611Thr
XM_011524859.1:c.1832T>C	XP_011523161.1:p.Met611Thr
XM_011524860.1:c.1829T>C	XP_011523162.1:p.Met610Thr
XM_011524861.1:c.1832T>C	XP_011523163.1:p.Met611Thr
XM_011524862.1:c.1166T>C	XP_011523164.1:p.Met389Thr