MyVariant.info:
GRCh37
chr1:g.115828756G>T
gnomAD v4:
Joint Max Group AF
0.00000183 (NFE)
Exomes Max Group AF
0.00000194 (NFE)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115286135G>T , CM000663.2:g.115286135G>T | GRCh38 |
| NC_000001.10:g.115828756G>T , CM000663.1:g.115828756G>T | GRCh37 |
| NC_000001.9:g.115630279G>T | NCBI36 |
| NG_007944.1:g.57102C>A , LRG_260:g.57102C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369512.3:c.661C>A (NGF) MANE Select | ENSP00000358525.2:p.Arg221= | |
| ENST00000675637.2:c.661C>A (NGF) | ENSP00000502831.1:p.Arg221= | |
| ENST00000676038.2:c.661C>A (NGF) | ENSP00000502380.1:p.Arg221= | |
| ENST00000679806.1:c.661C>A (NGF) | ENSP00000506492.1:p.Arg221= | |
| ENST00000680116.1:c.661C>A (NGF) | ENSP00000505694.1:p.Arg221= | |
| ENST00000680540.1:c.661C>A (NGF) | ENSP00000506569.1:p.Arg221= | |
| ENST00000680752.1:c.661C>A (NGF) | ENSP00000505558.1:p.Arg221= | |
| ENST00000681124.1:c.190C>A (NGF) | ENSP00000506364.1:p.Arg64= | |
| ENST00000369512.2:c.661C>A (NGF) | ENSP00000358525.2:p.Arg221= | |
| NM_002506.2:c.661C>A , LRG_260t1:c.661C>A (NGF) | NP_002497.2:p.Arg221= | |
| XM_006710663.2:c.661C>A (NGF) | XP_006710726.1:p.Arg221= | |
| XM_006710665.2:c.661C>A (NGF) | XP_006710728.1:p.Arg221= | |
| XM_011541518.1:c.826C>A (NGF) | XP_011539820.1:p.Arg276= | |
| NR_157569.1:n.207+2895G>T (NGF-AS1) | ||
| XM_006710663.3:c.661C>A (NGF) | XP_006710726.1:p.Arg221= | |
| XM_011541518.2:c.826C>A (NGF) | XP_011539820.1:p.Arg276= | |
| NM_002506.3:c.661C>A (NGF) MANE Select | NP_002497.2:p.Arg221= |