Linked Data
gnomAD v4:
2-26135066-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.26135068del , CM000664.2:g.26135068del | GRCh38 |
| NC_000002.11:g.26357937del , CM000664.1:g.26357937del | GRCh37 |
| NC_000002.10:g.26211441del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264710.5:c.*47del MANE Select | ENSP00000264710.4:n.*47del | |
| ENST00000264710.4:c.*47del | ENSP00000264710.4:n.*47del | |
| ENST00000473035.1:n.571del | ||
| ENST00000495146.5:n.1013del | ||
| NM_016131.4:c.*47del | NP_057215.3:n.*47del | |
| XM_024452565.1:c.*47del | XP_024308333.1:n.*47del | |
| NM_016131.5:c.*47del MANE Select | NP_057215.3:n.*47del |