Linked Data
gnomAD v4:
5-61332368-C-CGGT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.61332370_61332371insTGG , CM000667.2:g.61332370_61332371insTGG | GRCh38 |
| NC_000005.9:g.60628197_60628198insTGG , CM000667.1:g.60628197_60628198insTGG | GRCh37 |
| NC_000005.8:g.60663954_60663955insTGG | NCBI36 |
| NG_053150.1:g.5098_5099insTGG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252744.6:c.98_99insTGG MANE Select | ENSP00000252744.5:p.Gly33_Ala34insGly | |
| ENST00000252744.5:c.98_99insTGG | ENSP00000252744.5:p.Gly33_Ala34insGly | |
| NM_020928.1:c.98_99insTGG | NP_065979.1:p.Gly33_Ala34insGly | |
| NM_020928.2:c.98_99insTGG MANE Select | NP_065979.1:p.Gly33_Ala34insGly |