Linked Data
gnomAD v4:
6-1611804-C-CGGT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.1611806_1611807insTGG , CM000668.2:g.1611806_1611807insTGG | GRCh38 |
| NC_000006.11:g.1612041_1612042insTGG , CM000668.1:g.1612041_1612042insTGG | GRCh37 |
| NC_000006.10:g.1557040_1557041insTGG | NCBI36 |
| NG_009368.1:g.6361_6362insTGG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645831.2:c.1361_1362insTGG MANE Select | ENSP00000493906.1:p.Gly454_Gly455insGly | |
| ENST00000380874.3:c.1361_1362insTGG | ENSP00000370256.2:p.Gly454_Gly455insGly | |
| NM_001453.2:c.1361_1362insTGG | NP_001444.2:p.Gly454_Gly455insGly | |
| NM_001453.3:c.1361_1362insTGG MANE Select | NP_001444.2:p.Gly454_Gly455insGly |