Linked Data
ClinVar Variation Id:
2413874
ClinVar RCV Id:
RCV003104670
dbSNP Id:
rs1182195282
gnomAD v2:
15-80460440-G-A
gnomAD v3:
15-80168098-G-A
gnomAD v4:
15-80168098-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.80168098G>A , CM000677.2:g.80168098G>A | GRCh38 |
| NC_000015.9:g.80460440G>A , CM000677.1:g.80460440G>A | GRCh37 |
| NC_000015.8:g.78247495G>A | NCBI36 |
| NG_012833.1:g.20100G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682012.1:n.577G>A | ||
| ENST00000684569.1:n.547G>A | ||
| ENST00000561421.6:c.502G>A MANE Select | ENSP00000453347.2:p.Val168Met | |
| ENST00000646551.1:n.2129G>A | ||
| ENST00000261755.9:c.502G>A | ENSP00000261755.5:p.Val168Met | |
| ENST00000407106.5:c.502G>A | ENSP00000385080.1:p.Val168Met | |
| ENST00000539156.5:c.292G>A | ENSP00000454271.1:p.Val98Met | |
| ENST00000558514.1:n.48G>A | ||
| ENST00000558627.1:n.430G>A | ||
| ENST00000561421.5:c.502G>A | ENSP00000453347.1:p.Val168Met | |
| NM_000137.2:c.502G>A | NP_000128.1:p.Val168Met | |
| XM_024449872.1:c.502G>A | XP_024305640.1:p.Val168Met | |
| NM_000137.4:c.502G>A MANE Select | NP_000128.1:p.Val168Met | |
| NM_001374377.1:c.502G>A | NP_001361306.1:p.Val168Met | |
| NM_001374380.1:c.502G>A | NP_001361309.1:p.Val168Met |