Linked Data
ClinVar Variation Id:
386971
ClinVar RCV Id:
RCV000442787
dbSNP Id:
rs1045344879
gnomAD v3:
1-115293734-G-A
gnomAD v4:
1-115293734-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115293734G>A , CM000663.2:g.115293734G>A | GRCh38 |
| NC_000001.10:g.115836355G>A , CM000663.1:g.115836355G>A | GRCh37 |
| NC_000001.9:g.115637878G>A | NCBI36 |
| NG_007944.1:g.49503C>T , LRG_260:g.49503C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369512.3:c.-120C>T (NGF) MANE Select | ENSP00000358525.2:n.-120C>T | |
| ENST00000675637.2:c.-12-6927C>T (NGF) | ENSP00000502831.1:n.-12-6927C>T | |
| ENST00000676038.2:c.-120C>T (NGF) | ENSP00000502380.1:n.-120C>T | |
| ENST00000679806.1:c.-120C>T (NGF) | ENSP00000506492.1:n.-120C>T | |
| ENST00000680116.1:c.-590C>T (NGF) | ENSP00000505694.1:n.-590C>T | |
| ENST00000680752.1:c.-120C>T (NGF) | ENSP00000505558.1:n.-120C>T | |
| ENST00000681124.1:c.-528C>T (NGF) | ENSP00000506364.1:n.-528C>T | |
| ENST00000369512.2:c.-120C>T (NGF) | ENSP00000358525.2:n.-120C>T | |
| NM_002506.2:c.-120C>T , LRG_260t1:c.-120C>T (NGF) | NP_002497.2:n.-120C>T | |
| XM_006710663.2:c.-12-6927C>T (NGF) | XP_006710726.1:n.-12-6927C>T | |
| XM_006710665.2:c.-120C>T (NGF) | XP_006710728.1:n.-120C>T | |
| XM_011541518.1:c.46C>T (NGF) | XP_011539820.1:p.Arg16Cys | |
| NR_157569.1:n.207+10494G>A (NGF-AS1) | ||
| XM_006710663.3:c.-12-6927C>T (NGF) | XP_006710726.1:n.-12-6927C>T | |
| XM_011541518.2:c.46C>T (NGF) | XP_011539820.1:p.Arg16Cys | |
| NM_002506.3:c.-120C>T (NGF) MANE Select | NP_002497.2:n.-120C>T |