Linked Data
gnomAD v4:
10-94781885-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94781885A>G , CM000672.2:g.94781885A>G | GRCh38 |
| NC_000010.10:g.96541642A>G , CM000672.1:g.96541642A>G | GRCh37 |
| NC_000010.9:g.96531632A>G | NCBI36 |
| NG_008384.2:g.24180A>G | |
| NG_008384.3:g.24205A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.707A>G MANE Select | ENSP00000360372.3:p.Asn236Ser | |
| ENST00000645461.1:n.1760A>G | ||
| ENST00000371321.7:c.707A>G | ENSP00000360372.3:p.Asn236Ser | |
| ENST00000464755.1:c.1470A>G | ENSP00000483243.1:n.1470A>G | |
| NM_000769.2:c.707A>G | NP_000760.1:p.Asn236Ser | |
| NM_000769.4:c.707A>G MANE Select | NP_000760.1:p.Asn236Ser |