Linked Data
gnomAD v4:
10-122461632-G-GCCA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122461634_122461635insACC , CM000672.2:g.122461634_122461635insACC | GRCh38 |
| NC_000010.10:g.124221150_124221151insACC , CM000672.1:g.124221150_124221151insACC | GRCh37 |
| NC_000010.9:g.124211140_124211141insACC | NCBI36 |
| NG_011554.1:g.5110_5111insACC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.-19_-18insACC MANE Select | ENSP00000357980.3:n.-19_-18insACC | |
| ENST00000648167.1:c.154+2925_154+2926insACC | ENSP00000498033.1:n.154+2925_154+2926insACC | |
| ENST00000368984.7:c.-19_-18insACC | ENSP00000357980.3:n.-19_-18insACC | |
| NM_002775.4:c.-19_-18insACC | NP_002766.1:n.-19_-18insACC | |
| NM_002775.5:c.-19_-18insACC MANE Select | NP_002766.1:n.-19_-18insACC |