Linked Data
ClinVar Variation Id:
498710
dbSNP Id:
rs771853346
gnomAD v2:
5-127681121-C-T
gnomAD v3:
5-128345429-C-T
gnomAD v4:
5-128345429-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128345429C>T , CM000667.2:g.128345429C>T | GRCh38 |
| NC_000005.9:g.127681121C>T , CM000667.1:g.127681121C>T | GRCh37 |
| NC_000005.8:g.127709020C>T | NCBI36 |
| NG_008750.1:g.197615G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262464.9:c.3145G>A MANE Select | ENSP00000262464.4:p.Glu1049Lys | |
| ENST00000262464.8:c.3145G>A | ENSP00000262464.4:p.Glu1049Lys | |
| ENST00000508053.5:c.3145G>A | ENSP00000424571.1:p.Glu1049Lys | |
| ENST00000508989.5:c.3046G>A | ENSP00000425596.1:p.Glu1016Lys | |
| ENST00000619499.4:c.3142G>A | ENSP00000482132.1:p.Glu1048Lys | |
| NM_001999.3:c.3145G>A | NP_001990.2:p.Glu1049Lys | |
| XM_017009228.2:c.2992G>A | XP_016864717.1:p.Glu998Lys | |
| NM_001999.4:c.3145G>A MANE Select | NP_001990.2:p.Glu1049Lys |