Linked Data
dbSNP Id:
rs70957121
MyVariant Identifiers:
chr2:g.39939218_39939219insGTGTGA (hg19)
chr2:g.39712078_39712079insGTGTGA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.39712078_39712079insGTGTGA , CM000664.2:g.39712078_39712079insGTGTGA | GRCh38 |
| NC_000002.11:g.39939218_39939219insGTGTGA , CM000664.1:g.39939218_39939219insGTGTGA | GRCh37 |
| NC_000002.10:g.39792722_39792723insGTGTGA | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000281961.3:c.652+4892_652+4893insGTGTGA MANE Select | ENSP00000281961.2:n.652+4892_652+4893insGTGTGA | |
| ENST00000281961.2:c.652+4892_652+4893insGTGTGA | ENSP00000281961.2:n.652+4892_652+4893insGTGTGA | |
| ENST00000413011.5:n.371+4892_371+4893insGTGTGA | ||
| ENST00000482239.5:n.395+4892_395+4893insGTGTGA | ||
| ENST00000495402.1:n.431+4892_431+4893insGTGTGA | ||
| ENST00000618232.1:c.*42-4932_*42-4931insGTGTGA | ENSP00000477622.1:n.*42-4932_*42-4931insGTGTGA | |
| NM_001167959.1:c.106+4892_106+4893insGTGTGA | NP_001161431.1:n.106+4892_106+4893insGTGTGA | |
| NM_152390.2:c.652+4892_652+4893insGTGTGA | NP_689603.2:n.652+4892_652+4893insGTGTGA | |
| XM_005264144.1:c.515-4932_515-4931insGTGTGA | XP_005264201.1:n.515-4932_515-4931insGTGTGA | |
| XM_005264145.1:c.401-4932_401-4931insGTGTGA | XP_005264202.1:n.401-4932_401-4931insGTGTGA | |
| XM_017003369.1:c.*536_*537insGTGTGA | XP_016858858.1:n.*536_*537insGTGTGA | |
| XM_017003370.2:c.106+4892_106+4893insGTGTGA | XP_016858859.1:n.106+4892_106+4893insGTGTGA | |
| XM_017003371.1:c.106+4892_106+4893insGTGTGA | XP_016858860.1:n.106+4892_106+4893insGTGTGA | |
| XM_024452702.1:c.401-23151_401-23150insGTGTGA | XP_024308470.1:n.401-23151_401-23150insGTGTGA | |
| XM_024452703.1:c.106+4892_106+4893insGTGTGA | XP_024308471.1:n.106+4892_106+4893insGTGTGA | |
| XM_024452704.1:c.106+4892_106+4893insGTGTGA | XP_024308472.1:n.106+4892_106+4893insGTGTGA | |
| XM_024452705.1:c.106+4892_106+4893insGTGTGA | XP_024308473.1:n.106+4892_106+4893insGTGTGA | |
| NM_152390.3:c.652+4892_652+4893insGTGTGA MANE Select | NP_689603.2:n.652+4892_652+4893insGTGTGA | |
| NM_001167959.2:c.106+4892_106+4893insGTGTGA | NP_001161431.1:n.106+4892_106+4893insGTGTGA |