Canonical Allele Identifier: CA1023062

Gene: NGF NGF-AS1

Linked Data

• dbSNP Id: rs181709715
• ExAC: 1:115829277 G / T
• gnomAD v2: 1-115829277-G-T
• gnomAD v4: 1-115286656-G-T
• MyVariant Identifiers: chr1:g.115829277G>T (hg19) ; chr1:g.115286656G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115286656G>T , CM000663.2:g.115286656G>T	GRCh38
NC_000001.10:g.115829277G>T , CM000663.1:g.115829277G>T	GRCh37
NC_000001.9:g.115630800G>T	NCBI36
NG_007944.1:g.56581C>A , LRG_260:g.56581C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369512.3:c.140C>A (NGF) MANE Select	ENSP00000358525.2:p.Ala47Asp
ENST00000675637.2:c.140C>A (NGF)	ENSP00000502831.1:p.Ala47Asp
ENST00000676038.2:c.140C>A (NGF)	ENSP00000502380.1:p.Ala47Asp
ENST00000679806.1:c.140C>A (NGF)	ENSP00000506492.1:p.Ala47Asp
ENST00000680116.1:c.140C>A (NGF)	ENSP00000505694.1:p.Ala47Asp
ENST00000680540.1:c.140C>A (NGF)	ENSP00000506569.1:p.Ala47Asp
ENST00000680752.1:c.140C>A (NGF)	ENSP00000505558.1:p.Ala47Asp
ENST00000681124.1:c.-332C>A (NGF)	ENSP00000506364.1:n.-332C>A
ENST00000369512.2:c.140C>A (NGF)	ENSP00000358525.2:p.Ala47Asp
NM_002506.2:c.140C>A , LRG_260t1:c.140C>A (NGF)	NP_002497.2:p.Ala47Asp
XM_006710663.2:c.140C>A (NGF)	XP_006710726.1:p.Ala47Asp
XM_006710665.2:c.140C>A (NGF)	XP_006710728.1:p.Ala47Asp
XM_011541518.1:c.305C>A (NGF)	XP_011539820.1:p.Ala102Asp
NR_157569.1:n.207+3416G>T (NGF-AS1)
XM_006710663.3:c.140C>A (NGF)	XP_006710726.1:p.Ala47Asp
XM_011541518.2:c.305C>A (NGF)	XP_011539820.1:p.Ala102Asp
NM_002506.3:c.140C>A (NGF) MANE Select	NP_002497.2:p.Ala47Asp