Linked Data
ClinVar Variation Id:
213365
dbSNP Id:
rs768750542
ExAC:
5:127607765 T / C
gnomAD v2:
5-127607765-T-C
gnomAD v3:
5-128272073-T-C
gnomAD v4:
5-128272073-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128272073T>C , CM000667.2:g.128272073T>C | GRCh38 |
| NC_000005.9:g.127607765T>C , CM000667.1:g.127607765T>C | GRCh37 |
| NC_000005.8:g.127635664T>C | NCBI36 |
| NG_008750.1:g.270971A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703782.1:n.1A>G | ||
| ENST00000703783.1:n.4670A>G | ||
| ENST00000703784.1:n.53A>G | ||
| ENST00000262464.9:c.7886A>G MANE Select | ENSP00000262464.4:p.Gln2629Arg | |
| ENST00000262464.8:c.7886A>G | ENSP00000262464.4:p.Gln2629Arg | |
| ENST00000508053.5:c.7886A>G | ENSP00000424571.1:p.Gln2629Arg | |
| ENST00000619499.4:c.7883A>G | ENSP00000482132.1:p.Gln2628Arg | |
| NM_001999.3:c.7886A>G | NP_001990.2:p.Gln2629Arg | |
| XM_017009228.2:c.7733A>G | XP_016864717.1:p.Gln2578Arg | |
| NM_001999.4:c.7886A>G MANE Select | NP_001990.2:p.Gln2629Arg |