Linked Data
gnomAD v4:
10-133373229-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.133373229T>C , CM000672.2:g.133373229T>C | GRCh38 |
| NC_000010.10:g.135186733T>C , CM000672.1:g.135186733T>C | GRCh37 |
| NC_000010.9:g.135036723T>C | NCBI36 |
| NG_042077.1:g.5176A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368547.4:c.88+17A>G MANE Select | ENSP00000357535.3:n.88+17A>G | |
| ENST00000368547.3:c.88+17A>G | ENSP00000357535.3:n.88+17A>G | |
| NM_004092.3:c.88+17A>G | NP_004083.3:n.88+17A>G | |
| XR_002956965.1:n.151+17A>G | ||
| NM_004092.4:c.88+17A>G MANE Select | NP_004083.3:n.88+17A>G |