Linked Data
gnomAD v2:
19-40791298-T-TCCCCCCCCCC
gnomAD v3:
19-40285391-T-TCCCCCCCCCC
gnomAD v4:
19-40285391-T-TCCCCCCCCCC
MyVariant Identifiers:
chr19:g.40791298_40791299insCCCCCCCCCC (hg19)
chr19:g.40285391_40285392insCCCCCCCCCC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.40285394_40285395insCCCCCCCCCC , CM000681.2:g.40285394_40285395insCCCCCCCCCC | GRCh38 |
| NC_000019.9:g.40791301_40791302insCCCCCCCCCC , CM000681.1:g.40791301_40791302insCCCCCCCCCC | GRCh37 |
| NC_000019.8:g.45483141_45483142insCCCCCCCCCC | NCBI36 |
| NG_012038.2:g.4967_4968insGGGGGGGGGG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392038.6:c.-296_-295insGGGGGGGGGG | ENSP00000375892.2:n.-296_-295insGGGGGGGGGG | |
| ENST00000424901.5:c.-296_-295insGGGGGGGGGG | ENSP00000399532.2:n.-296_-295insGGGGGGGGGG | |
| ENST00000578123.5:c.-85+56_-85+57insGGGGGGGGGG | ENSP00000462022.1:n.-85+56_-85+57insGGGGGGGGGG | |
| NM_001243027.2:c.-445_-444insGGGGGGGGGG | NP_001229956.1:n.-445_-444insGGGGGGGGGG | |
| NM_001243028.2:c.-352_-351insGGGGGGGGGG | NP_001229957.1:n.-352_-351insGGGGGGGGGG | |
| NM_001626.5:c.-296_-295insGGGGGGGGGG | NP_001617.1:n.-296_-295insGGGGGGGGGG | |
| XM_011526620.1:c.-85+56_-85+57insGGGGGGGGGG | XP_011524922.1:n.-85+56_-85+57insGGGGGGGGGG |