Linked Data
ClinVar Variation Id:
1062788
dbSNP Id:
rs776098396
ExAC:
5:156021960 C / T
gnomAD v2:
5-156021960-C-T
gnomAD v3:
5-156594950-C-T
gnomAD v4:
5-156594950-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.156594950C>T , CM000667.2:g.156594950C>T | GRCh38 |
| NC_000005.9:g.156021960C>T , CM000667.1:g.156021960C>T | GRCh37 |
| NC_000005.8:g.155954538C>T | NCBI36 |
| NG_008693.2:g.729607C>T , LRG_205:g.729607C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000337851.9:c.401C>T MANE Select | ENSP00000338343.4:p.Ala134Val | |
| ENST00000337851.8:c.401C>T | ENSP00000338343.4:p.Ala134Val | |
| ENST00000435422.7:c.398C>T | ENSP00000403003.2:p.Ala133Val | |
| ENST00000517913.5:c.401C>T | ENSP00000429378.1:p.Ala134Val | |
| NM_000337.5:c.401C>T , LRG_205t1:c.401C>T | NP_000328.2:p.Ala134Val | |
| NM_001128209.1:c.398C>T | NP_001121681.1:p.Ala133Val | |
| NM_172244.2:c.401C>T | NP_758447.1:p.Ala134Val | |
| XM_005265966.3:c.401C>T | XP_005266023.1:p.Ala134Val | |
| XM_005265967.1:c.401C>T | XP_005266024.1:p.Ala134Val | |
| XM_006714911.2:c.401C>T | XP_006714974.1:p.Ala134Val | |
| XM_011534621.1:c.398C>T | XP_011532923.1:p.Ala133Val | |
| XM_005265966.5:c.401C>T | XP_005266023.1:p.Ala134Val | |
| XM_005265967.2:c.401C>T | XP_005266024.1:p.Ala134Val | |
| XM_011534621.2:c.398C>T | XP_011532923.1:p.Ala133Val | |
| XM_017009723.2:c.401C>T | XP_016865212.1:p.Ala134Val | |
| XM_017009724.1:c.401C>T | XP_016865213.1:p.Ala134Val | |
| NM_001128209.2:c.398C>T | NP_001121681.1:p.Ala133Val | |
| NM_172244.3:c.401C>T | NP_758447.1:p.Ala134Val | |
| NM_000337.6:c.401C>T MANE Select | NP_000328.2:p.Ala134Val |