Canonical Allele Identifier: CA1023030

Gene: NGF NGF-AS1

Linked Data

• dbSNP Id: rs760350868
• ExAC: 1:115829216 G / C
• gnomAD v2: 1-115829216-G-C
• gnomAD v4: 1-115286595-G-C
• MyVariant Identifiers: chr1:g.115829216G>C (hg19) ; chr1:g.115286595G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115286595G>C , CM000663.2:g.115286595G>C	GRCh38
NC_000001.10:g.115829216G>C , CM000663.1:g.115829216G>C	GRCh37
NC_000001.9:g.115630739G>C	NCBI36
NG_007944.1:g.56642C>G , LRG_260:g.56642C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000369512.3:c.201C>G (NGF) MANE Select	ENSP00000358525.2:p.Thr67=
ENST00000675637.2:c.201C>G (NGF)	ENSP00000502831.1:p.Thr67=
ENST00000676038.2:c.201C>G (NGF)	ENSP00000502380.1:p.Thr67=
ENST00000679806.1:c.201C>G (NGF)	ENSP00000506492.1:p.Thr67=
ENST00000680116.1:c.201C>G (NGF)	ENSP00000505694.1:p.Thr67=
ENST00000680540.1:c.201C>G (NGF)	ENSP00000506569.1:p.Thr67=
ENST00000680752.1:c.201C>G (NGF)	ENSP00000505558.1:p.Thr67=
ENST00000681124.1:c.-271C>G (NGF)	ENSP00000506364.1:n.-271C>G
ENST00000369512.2:c.201C>G (NGF)	ENSP00000358525.2:p.Thr67=
NM_002506.2:c.201C>G , LRG_260t1:c.201C>G (NGF)	NP_002497.2:p.Thr67=
XM_006710663.2:c.201C>G (NGF)	XP_006710726.1:p.Thr67=
XM_006710665.2:c.201C>G (NGF)	XP_006710728.1:p.Thr67=
XM_011541518.1:c.366C>G (NGF)	XP_011539820.1:p.Thr122=
NR_157569.1:n.207+3355G>C (NGF-AS1)
XM_006710663.3:c.201C>G (NGF)	XP_006710726.1:p.Thr67=
XM_011541518.2:c.366C>G (NGF)	XP_011539820.1:p.Thr122=
NM_002506.3:c.201C>G (NGF) MANE Select	NP_002497.2:p.Thr67=