Canonical Allele Identifier: CA727701095

Gene: NOS2

Linked Data

• dbSNP Id: rs563662307
• gnomAD v3: 17-27761670-C-A
• gnomAD v4: 17-27761670-C-A
• MyVariant Identifiers: chr17:g.26088696C>A (hg19) ; chr17:g.27761670C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27761670C>A , CM000679.2:g.27761670C>A	GRCh38
NC_000017.10:g.26088696C>A , CM000679.1:g.26088696C>A	GRCh37
NC_000017.9:g.23112823C>A	NCBI36
NG_011470.1:g.43860G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000697337.1:c.*3465-439G>T	ENSP00000513259.1:n.*3465-439G>T
ENST00000697338.1:c.2649-439G>T	ENSP00000513260.1:n.2649-439G>T
ENST00000697339.1:c.1763-439G>T	ENSP00000513261.1:n.1763-439G>T
ENST00000697340.1:c.*1514-439G>T	ENSP00000513262.1:n.*1514-439G>T
ENST00000313735.11:c.2801-439G>T MANE Select	ENSP00000327251.6:n.2801-439G>T
ENST00000646938.1:c.2798-439G>T	ENSP00000494870.1:n.2798-439G>T
ENST00000313735.10:c.2801-439G>T	ENSP00000327251.6:n.2801-439G>T
ENST00000621962.1:c.2684-439G>T	ENSP00000482291.1:n.2684-439G>T
NM_000625.4:c.2801-439G>T MANE Select	NP_000616.3:n.2801-439G>T
XM_011524859.1:c.2801-439G>T	XP_011523161.1:n.2801-439G>T
XM_011524860.1:c.2798-439G>T	XP_011523162.1:n.2798-439G>T
XM_011524861.1:c.2729-439G>T	XP_011523163.1:n.2729-439G>T
XM_011524862.1:c.2135-439G>T	XP_011523164.1:n.2135-439G>T