Linked Data
gnomAD v4:
10-94781848-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94781848G>A , CM000672.2:g.94781848G>A | GRCh38 |
| NC_000010.10:g.96541605G>A , CM000672.1:g.96541605G>A | GRCh37 |
| NC_000010.9:g.96531595G>A | NCBI36 |
| NG_008384.2:g.24143G>A | |
| NG_008384.3:g.24168G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.670G>A MANE Select | ENSP00000360372.3:p.Asp224Asn | |
| ENST00000645461.1:n.1723G>A | ||
| ENST00000371321.7:c.670G>A | ENSP00000360372.3:p.Asp224Asn | |
| ENST00000464755.1:c.1433G>A | ENSP00000483243.1:n.1433G>A | |
| NM_000769.2:c.670G>A | NP_000760.1:p.Asp224Asn | |
| NM_000769.4:c.670G>A MANE Select | NP_000760.1:p.Asp224Asn |