Canonical Allele Identifier: CA289063717

Gene: NOS2

Linked Data

• dbSNP Id: rs867504326
• gnomAD v3: 17-27783819-T-G
• gnomAD v4: 17-27783819-T-G
• MyVariant Identifiers: chr17:g.26110845T>G (hg19) ; chr17:g.27783819T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27783819T>G , CM000679.2:g.27783819T>G	GRCh38
NC_000017.10:g.26110845T>G , CM000679.1:g.26110845T>G	GRCh37
NC_000017.9:g.23134972T>G	NCBI36
NG_011470.1:g.21711A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000697337.1:c.319-713A>C	ENSP00000513259.1:n.319-713A>C
ENST00000697338.1:c.316-713A>C	ENSP00000513260.1:n.316-713A>C
ENST00000697339.1:c.315+4990A>C	ENSP00000513261.1:n.315+4990A>C
ENST00000697340.1:c.465-713A>C	ENSP00000513262.1:n.465-713A>C
ENST00000697341.1:n.438-713A>C
ENST00000313735.11:c.468-713A>C MANE Select	ENSP00000327251.6:n.468-713A>C
ENST00000646938.1:c.465-713A>C	ENSP00000494870.1:n.465-713A>C
ENST00000313735.10:c.468-713A>C	ENSP00000327251.6:n.468-713A>C
ENST00000621962.1:c.468-713A>C	ENSP00000482291.1:n.468-713A>C
NM_000625.4:c.468-713A>C MANE Select	NP_000616.3:n.468-713A>C
XM_011524859.1:c.468-713A>C	XP_011523161.1:n.468-713A>C
XM_011524860.1:c.465-713A>C	XP_011523162.1:n.465-713A>C
XM_011524861.1:c.468-713A>C	XP_011523163.1:n.468-713A>C
XM_011524862.1:c.-199-713A>C	XP_011523164.1:n.-199-713A>C