Linked Data
gnomAD v4:
10-44385998-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.44385998C>A , CM000672.2:g.44385998C>A | GRCh38 |
| NC_000010.10:g.44881446C>A , CM000672.1:g.44881446C>A | GRCh37 |
| NC_000010.9:g.44201452C>A | NCBI36 |
| NG_016861.1:g.4100G>T | |
| NG_016861.2:g.4100G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496375.1:n.496G>T |