Linked Data
gnomAD v4:
3-129531139-T-TACTG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129531139_129531140insACTG , CM000665.2:g.129531139_129531140insACTG | GRCh38 |
| NC_000003.11:g.129249982_129249983insACTG , CM000665.1:g.129249982_129249983insACTG | GRCh37 |
| NC_000003.10:g.130732672_130732673insACTG | NCBI36 |
| NG_009115.1:g.7501_7502insACTG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296271.4:c.530+95_530+96insACTG MANE Select | ENSP00000296271.3:n.530+95_530+96insACTG | |
| ENST00000296271.3:c.530+95_530+96insACTG | ENSP00000296271.3:n.530+95_530+96insACTG | |
| NM_000539.3:c.530+95_530+96insACTG MANE Select | NP_000530.1:n.530+95_530+96insACTG |