Canonical Allele Identifier: CA1023046

Gene: NGF NGF-AS1

Linked Data

• ClinVar Variation Id: 456627
• ClinVar RCV Id: RCV000553133 ; RCV004553172 ; RCV002413446
• dbSNP Id: rs201861727
• ExAC: 1:115829244 G / A
• gnomAD v2: 1-115829244-G-A
• gnomAD v3: 1-115286623-G-A
• gnomAD v4: 1-115286623-G-A
• COSMIC: COSM4020977
• MyVariant Identifiers: chr1:g.115829244G>A (hg19) ; chr1:g.115286623G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115286623G>A , CM000663.2:g.115286623G>A	GRCh38
NC_000001.10:g.115829244G>A , CM000663.1:g.115829244G>A	GRCh37
NC_000001.9:g.115630767G>A	NCBI36
NG_007944.1:g.56614C>T , LRG_260:g.56614C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369512.3:c.173C>T (NGF) MANE Select	ENSP00000358525.2:p.Ala58Val
ENST00000675637.2:c.173C>T (NGF)	ENSP00000502831.1:p.Ala58Val
ENST00000676038.2:c.173C>T (NGF)	ENSP00000502380.1:p.Ala58Val
ENST00000679806.1:c.173C>T (NGF)	ENSP00000506492.1:p.Ala58Val
ENST00000680116.1:c.173C>T (NGF)	ENSP00000505694.1:p.Ala58Val
ENST00000680540.1:c.173C>T (NGF)	ENSP00000506569.1:p.Ala58Val
ENST00000680752.1:c.173C>T (NGF)	ENSP00000505558.1:p.Ala58Val
ENST00000681124.1:c.-299C>T (NGF)	ENSP00000506364.1:n.-299C>T
ENST00000369512.2:c.173C>T (NGF)	ENSP00000358525.2:p.Ala58Val
NM_002506.2:c.173C>T , LRG_260t1:c.173C>T (NGF)	NP_002497.2:p.Ala58Val
XM_006710663.2:c.173C>T (NGF)	XP_006710726.1:p.Ala58Val
XM_006710665.2:c.173C>T (NGF)	XP_006710728.1:p.Ala58Val
XM_011541518.1:c.338C>T (NGF)	XP_011539820.1:p.Ala113Val
NR_157569.1:n.207+3383G>A (NGF-AS1)
XM_006710663.3:c.173C>T (NGF)	XP_006710726.1:p.Ala58Val
XM_011541518.2:c.338C>T (NGF)	XP_011539820.1:p.Ala113Val
NM_002506.3:c.173C>T (NGF) MANE Select	NP_002497.2:p.Ala58Val