Linked Data
ClinVar Variation Id:
4823
ClinVar RCV Id:
RCV000005092
dbSNP Id:
rs121908364
gnomAD v4:
7-107689166-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107689166C>T , CM000669.2:g.107689166C>T | GRCh38 |
| NC_000007.13:g.107329611C>T , CM000669.1:g.107329611C>T | GRCh37 |
| NC_000007.12:g.107116847C>T | NCBI36 |
| NG_008489.1:g.33532C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644269.2:c.1115C>T MANE Select | ENSP00000494017.1:p.Ala372Val | |
| ENST00000265715.7:c.1115C>T | ENSP00000265715.3:p.Ala372Val | |
| NM_000441.1:c.1115C>T | NP_000432.1:p.Ala372Val | |
| XM_005250425.1:c.1115C>T | XP_005250482.1:p.Ala372Val | |
| XM_006716025.2:c.1115C>T | XP_006716088.1:p.Ala372Val | |
| XM_005250425.2:c.1115C>T | XP_005250482.1:p.Ala372Val | |
| XM_006716025.3:c.1115C>T | XP_006716088.1:p.Ala372Val | |
| XM_017012318.1:c.1115C>T | XP_016867807.1:p.Ala372Val | |
| NM_000441.2:c.1115C>T MANE Select | NP_000432.1:p.Ala372Val |