Linked Data
gnomAD v4:
10-44386222-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.44386222T>C , CM000672.2:g.44386222T>C | GRCh38 |
| NC_000010.10:g.44881670T>C , CM000672.1:g.44881670T>C | GRCh37 |
| NC_000010.9:g.44201676T>C | NCBI36 |
| NG_016861.1:g.3876A>G | |
| NG_016861.2:g.3876A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496375.1:n.272A>G |