Canonical Allele Identifier: CA1023038

Gene: NGF NGF-AS1

Linked Data

• ClinVar Variation Id: 1024609
• ClinVar RCV Id: RCV001324816
• dbSNP Id: rs750829893
• ExAC: 1:115829230 C / T
• gnomAD v2: 1-115829230-C-T
• gnomAD v3: 1-115286609-C-T
• gnomAD v4: 1-115286609-C-T
• MyVariant Identifiers: chr1:g.115829230C>T (hg19) ; chr1:g.115286609C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115286609C>T , CM000663.2:g.115286609C>T	GRCh38
NC_000001.10:g.115829230C>T , CM000663.1:g.115829230C>T	GRCh37
NC_000001.9:g.115630753C>T	NCBI36
NG_007944.1:g.56628G>A , LRG_260:g.56628G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369512.3:c.187G>A (NGF) MANE Select	ENSP00000358525.2:p.Val63Met
ENST00000675637.2:c.187G>A (NGF)	ENSP00000502831.1:p.Val63Met
ENST00000676038.2:c.187G>A (NGF)	ENSP00000502380.1:p.Val63Met
ENST00000679806.1:c.187G>A (NGF)	ENSP00000506492.1:p.Val63Met
ENST00000680116.1:c.187G>A (NGF)	ENSP00000505694.1:p.Val63Met
ENST00000680540.1:c.187G>A (NGF)	ENSP00000506569.1:p.Val63Met
ENST00000680752.1:c.187G>A (NGF)	ENSP00000505558.1:p.Val63Met
ENST00000681124.1:c.-285G>A (NGF)	ENSP00000506364.1:n.-285G>A
ENST00000369512.2:c.187G>A (NGF)	ENSP00000358525.2:p.Val63Met
NM_002506.2:c.187G>A , LRG_260t1:c.187G>A (NGF)	NP_002497.2:p.Val63Met
XM_006710663.2:c.187G>A (NGF)	XP_006710726.1:p.Val63Met
XM_006710665.2:c.187G>A (NGF)	XP_006710728.1:p.Val63Met
XM_011541518.1:c.352G>A (NGF)	XP_011539820.1:p.Val118Met
NR_157569.1:n.207+3369C>T (NGF-AS1)
XM_006710663.3:c.187G>A (NGF)	XP_006710726.1:p.Val63Met
XM_011541518.2:c.352G>A (NGF)	XP_011539820.1:p.Val118Met
NM_002506.3:c.187G>A (NGF) MANE Select	NP_002497.2:p.Val63Met