Canonical Allele Identifier: CA2636788988

Gene: NOS2

Linked Data

• gnomAD v4: 17-27772179-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27772179C>A , CM000679.2:g.27772179C>A	GRCh38
NC_000017.10:g.26099205C>A , CM000679.1:g.26099205C>A	GRCh37
NC_000017.9:g.23123332C>A	NCBI36
NG_011470.1:g.33351G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000697337.1:c.*1279G>T	ENSP00000513259.1:n.*1279G>T
ENST00000697338.1:c.1552+129G>T	ENSP00000513260.1:n.1552+129G>T
ENST00000697339.1:c.738+129G>T	ENSP00000513261.1:n.738+129G>T
ENST00000697340.1:c.*421+129G>T	ENSP00000513262.1:n.*421+129G>T
ENST00000697341.1:n.1674+129G>T
ENST00000313735.11:c.1704+129G>T MANE Select	ENSP00000327251.6:n.1704+129G>T
ENST00000646938.1:c.1701+129G>T	ENSP00000494870.1:n.1701+129G>T
ENST00000313735.10:c.1704+129G>T	ENSP00000327251.6:n.1704+129G>T
ENST00000621962.1:c.1587+129G>T	ENSP00000482291.1:n.1587+129G>T
NM_000625.4:c.1704+129G>T MANE Select	NP_000616.3:n.1704+129G>T
XM_011524859.1:c.1704+129G>T	XP_011523161.1:n.1704+129G>T
XM_011524860.1:c.1701+129G>T	XP_011523162.1:n.1701+129G>T
XM_011524861.1:c.1704+129G>T	XP_011523163.1:n.1704+129G>T
XM_011524862.1:c.1038+129G>T	XP_011523164.1:n.1038+129G>T