Linked Data
gnomAD v4:
10-44385968-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.44385968T>C , CM000672.2:g.44385968T>C | GRCh38 |
| NC_000010.10:g.44881416T>C , CM000672.1:g.44881416T>C | GRCh37 |
| NC_000010.9:g.44201422T>C | NCBI36 |
| NG_016861.1:g.4130A>G | |
| NG_016861.2:g.4130A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496375.1:n.518+8A>G |