Linked Data
dbSNP Id:
rs34359946
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23420809dup , CM000676.2:g.23420809dup | GRCh38 |
| NC_000014.8:g.23890018dup , CM000676.1:g.23890018dup | GRCh37 |
| NC_000014.7:g.22959858dup | NCBI36 |
| NG_007884.1:g.19854dup , LRG_384:g.19854dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.3336+150dup MANE Select | ENSP00000347507.3:n.3336+150dup | |
| ENST00000355349.3:c.3336+150dup | ENSP00000347507.3:n.3336+150dup | |
| NM_000257.3:c.3336+150dup | NP_000248.2:n.3336+150dup | |
| XR_245686.3:n.3444+150dup | ||
| XM_017021340.1:c.3336+150dup | XP_016876829.1:n.3336+150dup | |
| NM_000257.4:c.3336+150dup MANE Select | NP_000248.2:n.3336+150dup |