Linked Data
gnomAD v4:
10-44386072-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.44386072A>G , CM000672.2:g.44386072A>G | GRCh38 |
| NC_000010.10:g.44881520A>G , CM000672.1:g.44881520A>G | GRCh37 |
| NC_000010.9:g.44201526A>G | NCBI36 |
| NG_016861.1:g.4026T>C | |
| NG_016861.2:g.4026T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496375.1:n.422T>C |