Linked Data
gnomAD v4:
1-152305030-G-GC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.152305030_152305031insC , CM000663.2:g.152305030_152305031insC | GRCh38 |
| NC_000001.10:g.152277506_152277507insC , CM000663.1:g.152277506_152277507insC | GRCh37 |
| NC_000001.9:g.150544130_150544131insC | NCBI36 |
| NG_016190.1:g.25173_25174insG , LRG_1028:g.25173_25174insG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368799.2:c.9855_9856insG MANE Select | ENSP00000357789.1:p.Gln3286AlafsTer7 | |
| ENST00000368799.1:c.9855_9856insG | ENSP00000357789.1:p.Gln3286AlafsTer7 | |
| NM_002016.1:c.9855_9856insG , LRG_1028t1:c.9855_9856insG | NP_002007.1:p.Gln3286AlafsTer7 | |
| XM_011509329.1:c.9108+747_9108+748insG | XP_011507631.1:n.9108+747_9108+748insG | |
| NM_002016.2:c.9855_9856insG MANE Select | NP_002007.1:p.Gln3286AlafsTer7 |