Linked Data
gnomAD v4:
10-133538898-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.133538898C>G , CM000672.2:g.133538898C>G | GRCh38 |
| NC_000010.10:g.135352402C>G , CM000672.1:g.135352402C>G | GRCh37 |
| NC_000010.9:g.135202392C>G | NCBI36 |
| NG_008383.1:g.16536C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252945.8:c.1416C>G MANE Select | ENSP00000252945.3:p.Ser472Arg | |
| ENST00000252945.7:c.1416C>G | ENSP00000252945.3:p.Ser472Arg | |
| ENST00000368520.1:n.1358+1006C>G | ||
| ENST00000463117.6:c.1416C>G | ENSP00000440689.1:p.Ser472Arg | |
| ENST00000469258.1:n.512C>G | ||
| NM_000773.3:c.1416C>G | NP_000764.1:p.Ser472Arg | |
| NM_000773.4:c.1416C>G MANE Select | NP_000764.1:p.Ser472Arg |