Linked Data
dbSNP Id:
rs372502477
gnomAD v3:
10-62528638-G-GGAA
gnomAD v4:
10-62528638-G-GGAA
MyVariant Identifiers:
chr10:g.64288397_64288398insGAA (hg19)
chr10:g.62528638_62528639insGAA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.62528638_62528639insGAA , CM000672.2:g.62528638_62528639insGAA | GRCh38 |
| NC_000010.10:g.64288397_64288398insGAA , CM000672.1:g.64288397_64288398insGAA | GRCh37 |
| NC_000010.9:g.63958403_63958404insGAA | NCBI36 |
| NG_021209.1:g.159482_159483insGAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647733.1:c.981+68841_981+68842insGAA | ENSP00000502188.1:n.981+68841_981+68842insGAA | |
| ENST00000395251.5:c.-185+8041_-185+8042insGAA | ENSP00000378672.1:n.-185+8041_-185+8042insGAA | |
| ENST00000410046.7:c.981+68841_981+68842insGAA | ENSP00000387091.3:n.981+68841_981+68842insGAA | |
| NM_199451.2:c.981+68841_981+68842insGAA | NP_955523.1:n.981+68841_981+68842insGAA | |
| NM_199452.3:c.-185+8041_-185+8042insGAA | NP_955524.3:n.-185+8041_-185+8042insGAA | |
| XM_017015937.2:c.982-15571_982-15570insGAA | XP_016871426.1:n.982-15571_982-15570insGAA | |
| NM_199451.3:c.981+68841_981+68842insGAA | NP_955523.1:n.981+68841_981+68842insGAA |