Linked Data
dbSNP Id:
rs772810680
ExAC:
15:75013017 C / A
gnomAD v2:
15-75013017-C-A
gnomAD v4:
15-74720676-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74720676C>A , CM000677.2:g.74720676C>A | GRCh38 |
| NC_000015.9:g.75013017C>A , CM000677.1:g.75013017C>A | GRCh37 |
| NC_000015.8:g.72800070C>A | NCBI36 |
| NG_008431.1:g.3135C>A | |
| NG_008431.2:g.3135C>A | |
| NG_061374.1:g.9853G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379727.8:c.1352G>T MANE Select | ENSP00000369050.3:p.Gly451Val | |
| ENST00000379727.7:c.1352G>T | ENSP00000369050.3:p.Gly451Val | |
| ENST00000395048.6:c.1352G>T | ENSP00000378488.2:p.Gly451Val | |
| ENST00000395049.8:c.1265G>T | ENSP00000378489.4:p.Gly422Val | |
| ENST00000567032.5:c.1352G>T | ENSP00000456585.1:p.Gly451Val | |
| ENST00000612821.4:c.1268G>T | ENSP00000479744.1:p.Gly423Val | |
| ENST00000617691.4:c.1265G>T | ENSP00000482863.1:p.Gly422Val | |
| NM_000499.3:c.1352G>T | NP_000490.1:p.Gly451Val | |
| XM_005254185.1:c.1352G>T | XP_005254242.1:p.Gly451Val | |
| NM_000499.5:c.1352G>T | NP_000490.1:p.Gly451Val | |
| NM_001319216.2:c.1265G>T | NP_001306145.1:p.Gly422Val | |
| NM_001319217.2:c.1352G>T MANE Select | NP_001306146.1:p.Gly451Val |