Linked Data
dbSNP Id:
rs1474046404
gnomAD v2:
19-38778780-G-GC
gnomAD v3:
19-38288140-G-GC
gnomAD v4:
19-38288140-G-GC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38288142dup , CM000681.2:g.38288142dup | GRCh38 |
| NC_000019.9:g.38778782dup , CM000681.1:g.38778782dup | GRCh37 |
| NC_000019.8:g.43470622dup | NCBI36 |
| NG_013372.1:g.28685dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301244.12:c.337+207dup MANE Select | ENSP00000301244.5:n.337+207dup | |
| ENST00000301244.11:c.337+207dup | ENSP00000301244.5:n.337+207dup | |
| ENST00000454580.7:c.166+207dup | ENSP00000389788.2:n.166+207dup | |
| ENST00000587090.5:c.187+207dup | ENSP00000466407.1:n.187+207dup | |
| ENST00000587516.5:c.278-996dup | ENSP00000465721.1:n.278-996dup | |
| NM_001166103.1:c.166+207dup | NP_001159575.1:n.166+207dup | |
| NM_021102.3:c.337+207dup | NP_066925.1:n.337+207dup | |
| NM_021102.4:c.337+207dup MANE Select | NP_066925.1:n.337+207dup | |
| NM_001166103.2:c.166+207dup | NP_001159575.1:n.166+207dup |