Linked Data
ClinVar Variation Id:
2749330
ClinVar RCV Id:
RCV003497825
MyVariant Identifiers:
chr1:g.183532652C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.183563517C>T , CM000663.2:g.183563517C>T | GRCh38 |
| NC_000001.10:g.183532652C>T , CM000663.1:g.183532652C>T | GRCh37 |
| NC_000001.9:g.181799275C>T | NCBI36 |
| NG_007267.1:g.32065G>A , LRG_88:g.32065G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000469280.2:n.535G>A (NCF2) | ||
| ENST00000697329.1:n.1015G>A (NCF2) | ||
| ENST00000697330.1:c.1095G>A (NCF2) | ENSP00000513258.1:p.Lys365= | |
| ENST00000697351.1:c.987G>A (NCF2) | ENSP00000513276.1:p.Lys329= | |
| ENST00000367535.8:c.1095G>A (NCF2) MANE Select | ENSP00000356505.4:p.Lys365= | |
| ENST00000367535.7:c.1095G>A (NCF2) | ENSP00000356505.3:p.Lys365= | |
| ENST00000367536.5:c.1095G>A (NCF2) | ENSP00000356506.1:p.Lys365= | |
| ENST00000413720.5:c.960G>A (NCF2) | ENSP00000399294.1:p.Lys320= | |
| ENST00000418089.5:c.852G>A (NCF2) | ENSP00000407217.1:p.Lys284= | |
| ENST00000419402.1:c.312G>A (NCF2) | ENSP00000406198.1:p.Lys104= | |
| ENST00000420553.5:c.48G>A (NCF2) | ENSP00000397228.1:p.Lys16= | |
| ENST00000469280.1:n.535G>A (NCF2) | ||
| ENST00000495321.1:n.233+12327C>T (SMG7) | ||
| NM_000433.3:c.1095G>A , LRG_88t1:c.1095G>A (NCF2) | NP_000424.2:p.Lys365= | |
| NM_001127651.2:c.1095G>A (NCF2) | NP_001121123.1:p.Lys365= | |
| NM_001190789.1:c.852G>A (NCF2) | NP_001177718.1:p.Lys284= | |
| NM_001190794.1:c.960G>A (NCF2) | NP_001177723.1:p.Lys320= | |
| XM_005245207.1:c.987G>A (NCF2) | XP_005245264.1:p.Lys329= | |
| XM_011509580.1:c.1095G>A (NCF2) | XP_011507882.1:p.Lys365= | |
| XM_011509581.1:c.1095G>A (NCF2) | XP_011507883.1:p.Lys365= | |
| XR_921801.1:n.1157G>A (NCF2) | ||
| NM_000433.4:c.1095G>A (NCF2) MANE Select | NP_000424.2:p.Lys365= | |
| NM_001127651.3:c.1095G>A (NCF2) | NP_001121123.1:p.Lys365= | |
| NM_001190789.2:c.852G>A (NCF2) | NP_001177718.1:p.Lys284= | |
| NM_001190794.2:c.960G>A (NCF2) | NP_001177723.1:p.Lys320= |