Linked Data
gnomAD v4:
X-68829756-G-GTGCAGTCT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.68829757_68829764dup , CM000685.2:g.68829757_68829764dup | GRCh38 |
| NC_000023.10:g.68049600_68049607dup , CM000685.1:g.68049600_68049607dup | GRCh37 |
| NC_000023.9:g.67966325_67966332dup | NCBI36 |
| NG_008887.1:g.5761_5768dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000204961.5:c.-20_-13dup MANE Select | ENSP00000204961.4:n.-20_-13dup | |
| ENST00000204961.4:c.-20_-13dup | ENSP00000204961.4:n.-20_-13dup | |
| NM_004429.4:c.-20_-13dup | NP_004420.1:n.-20_-13dup | |
| NM_004429.5:c.-20_-13dup MANE Select | NP_004420.1:n.-20_-13dup |