Linked Data
gnomAD v4:
18-31524683-C-CA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31524684dup , CM000680.2:g.31524684dup | GRCh38 |
| NC_000018.9:g.29104647dup , CM000680.1:g.29104647dup | GRCh37 |
| NC_000018.8:g.27358645dup | NCBI36 |
| NG_007072.3:g.31443dup , LRG_397:g.31443dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000682087.2:n.660-19dup | ||
| ENST00000683614.2:n.660-19dup | ||
| ENST00000682087.1:c.660-19dup | ||
| ENST00000683614.1:c.660-19dup | ||
| ENST00000261590.13:c.829-19dup MANE Select | ENSP00000261590.8:n.829-19dup | |
| ENST00000261590.12:c.829-19dup | ENSP00000261590.8:n.829-19dup | |
| NM_001943.3:c.829-19dup , LRG_397t1:c.829-19dup | NP_001934.2:n.829-19dup | |
| NM_001943.4:c.829-19dup | NP_001934.2:n.829-19dup | |
| XM_024451095.1:c.295-19dup | XP_024306863.1:n.295-19dup | |
| NM_001943.5:c.829-19dup MANE Select | NP_001934.2:n.829-19dup |