Canonical Allele Identifier: CA10737260
Gene: NGF HGNC NCBI
NGF-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.115338434G>A
GRCh37 chr1:g.115881055G>A
gnomAD v2:
1:115881055 G / A
gnomAD v3:
1:115338434 G / A
gnomAD v4:
chr1-115338434-G-A
Joint Max Group AF 0.64363881 (NFE)
Genomes Max Group AF 0.64363881 (NFE)
ClinVar RCV:
RCV000826444
ClinVar Variation:
667672
dbSNP:
11102930
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115338434G>A , CM000663.2:g.115338434G>A GRCh38
NC_000001.10:g.115881055G>A , CM000663.1:g.115881055G>A GRCh37
NC_000001.9:g.115682578G>A NCBI36
NG_007944.1:g.4803C>T , LRG_260:g.4803C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000679806.1:c.-137+174C>T (NGF) ENSP00000506492.1:n.-137+174C>T
ENST00000680752.1:c.-206C>T (NGF) ENSP00000505558.1:n.-206C>T
NR_157569.1:n.208-27236G>A (NGF-AS1)
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