Linked Data
gnomAD v4:
2-26135394-C-CA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.26135395dup , CM000664.2:g.26135395dup | GRCh38 |
| NC_000002.11:g.26358264dup , CM000664.1:g.26358264dup | GRCh37 |
| NC_000002.10:g.26211768dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264710.5:c.*374dup MANE Select | ENSP00000264710.4:n.*374dup | |
| ENST00000264710.4:c.*374dup | ENSP00000264710.4:n.*374dup | |
| NM_016131.4:c.*374dup | NP_057215.3:n.*374dup | |
| XM_024452565.1:c.*374dup | XP_024308333.1:n.*374dup | |
| NM_016131.5:c.*374dup MANE Select | NP_057215.3:n.*374dup |