Canonical Allele Identifier: CA29767767

Gene: NGF NGF-AS1

Linked Data

• ClinVar Variation Id: 526752
• ClinVar RCV Id: RCV000631365
• dbSNP Id: rs1014644520
• gnomAD v2: 1-115829324-G-C
• gnomAD v3: 1-115286703-G-C
• gnomAD v4: 1-115286703-G-C
• MyVariant Identifiers: chr1:g.115829324G>C (hg19) ; chr1:g.115286703G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115286703G>C , CM000663.2:g.115286703G>C	GRCh38
NC_000001.10:g.115829324G>C , CM000663.1:g.115829324G>C	GRCh37
NC_000001.9:g.115630847G>C	NCBI36
NG_007944.1:g.56534C>G , LRG_260:g.56534C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000369512.3:c.93C>G (NGF) MANE Select	ENSP00000358525.2:p.Thr31=
ENST00000675637.2:c.93C>G (NGF)	ENSP00000502831.1:p.Thr31=
ENST00000676038.2:c.93C>G (NGF)	ENSP00000502380.1:p.Thr31=
ENST00000679806.1:c.93C>G (NGF)	ENSP00000506492.1:p.Thr31=
ENST00000680116.1:c.93C>G (NGF)	ENSP00000505694.1:p.Thr31=
ENST00000680540.1:c.93C>G (NGF)	ENSP00000506569.1:p.Thr31=
ENST00000680752.1:c.93C>G (NGF)	ENSP00000505558.1:p.Thr31=
ENST00000681124.1:c.-379C>G (NGF)	ENSP00000506364.1:n.-379C>G
ENST00000369512.2:c.93C>G (NGF)	ENSP00000358525.2:p.Thr31=
NM_002506.2:c.93C>G , LRG_260t1:c.93C>G (NGF)	NP_002497.2:p.Thr31=
XM_006710663.2:c.93C>G (NGF)	XP_006710726.1:p.Thr31=
XM_006710665.2:c.93C>G (NGF)	XP_006710728.1:p.Thr31=
XM_011541518.1:c.258C>G (NGF)	XP_011539820.1:p.Thr86=
NR_157569.1:n.207+3463G>C (NGF-AS1)
XM_006710663.3:c.93C>G (NGF)	XP_006710726.1:p.Thr31=
XM_011541518.2:c.258C>G (NGF)	XP_011539820.1:p.Thr86=
NM_002506.3:c.93C>G (NGF) MANE Select	NP_002497.2:p.Thr31=