Linked Data
ClinVar Variation Id:
908417
dbSNP Id:
rs775377530
ExAC:
8:134145791 C / T
gnomAD v2:
8-134145791-C-T
gnomAD v3:
8-133133547-C-T
gnomAD v4:
8-133133547-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.133133547C>T , CM000670.2:g.133133547C>T | GRCh38 |
| NC_000008.10:g.134145791C>T , CM000670.1:g.134145791C>T | GRCh37 |
| NC_000008.9:g.134214973C>T | NCBI36 |
| NG_015832.1:g.271587C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000220616.9:c.8075C>T MANE Select | ENSP00000220616.4:p.Ala2692Val | |
| ENST00000220616.8:c.8075C>T | ENSP00000220616.4:p.Ala2692Val | |
| ENST00000519178.5:c.3441C>T | ||
| ENST00000519543.5:c.2474C>T | ENSP00000430430.1:p.Ala825Val | |
| ENST00000521107.1:c.287C>T | ENSP00000430161.1:p.Ala96Val | |
| ENST00000522691.1:n.161C>T | ||
| ENST00000523756.5:c.4730C>T | ||
| NM_003235.4:c.8075C>T | NP_003226.4:p.Ala2692Val | |
| XM_005251038.3:c.7883C>T | XP_005251095.1:p.Ala2628Val | |
| XM_006716622.2:c.8012C>T | XP_006716685.1:p.Ala2671Val | |
| XM_005251038.4:c.7883C>T | XP_005251095.1:p.Ala2628Val | |
| XM_006716622.3:c.8012C>T | XP_006716685.1:p.Ala2671Val | |
| XM_017013793.1:c.8009C>T | XP_016869282.1:p.Ala2670Val | |
| XM_017013794.1:c.7940C>T | XP_016869283.1:p.Ala2647Val | |
| XM_017013795.1:c.7904C>T | XP_016869284.1:p.Ala2635Val | |
| XM_017013796.1:c.7856C>T | XP_016869285.1:p.Ala2619Val | |
| XM_017013797.1:c.7814C>T | XP_016869286.1:p.Ala2605Val | |
| NM_003235.5:c.8075C>T MANE Select | NP_003226.4:p.Ala2692Val |