Linked Data
gnomAD v4:
10-44370518-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.44370520del , CM000672.2:g.44370520del | GRCh38 |
| NC_000010.10:g.44865968del , CM000672.1:g.44865968del | GRCh37 |
| NC_000010.9:g.44185974del | NCBI36 |
| NG_016861.1:g.19579del | |
| NG_016861.2:g.19579del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374429.6:c.*2809del | ENSP00000363551.2:n.*2809del | |
| NM_000609.6:c.*2809del | NP_000600.1:n.*2809del | |
| NM_001277990.1:c.*2369del | NP_001264919.1:n.*2369del | |
| XR_001747171.1:n.331+8118del | ||
| XR_001747172.1:n.331+8118del | ||
| XR_001747173.1:n.331+8118del | ||
| XR_001747174.1:n.331+8118del | ||
| NM_000609.7:c.*2809del | NP_000600.1:n.*2809del | |
| NM_001277990.2:c.*2369del | NP_001264919.1:n.*2369del |