Linked Data
gnomAD v4:
3-138945889-TCC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.138945891_138945892del , CM000665.2:g.138945891_138945892del | GRCh38 |
| NC_000003.11:g.138664733_138664734del , CM000665.1:g.138664733_138664734del | GRCh37 |
| NC_000003.10:g.140147423_140147424del | NCBI36 |
| NG_012454.1:g.6250_6251del | |
| NG_029796.1:g.3658_3659del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648323.1:c.832_833del MANE Select | ENSP00000497217.1:p.Gly278ArgfsTer? | |
| ENST00000330315.3:c.832_833del | ENSP00000333188.3:p.Gly278ArgfsTer? | |
| NM_023067.3:c.832_833del | NP_075555.1:p.Gly278ArgfsTer? | |
| NM_023067.4:c.832_833del MANE Select | NP_075555.1:p.Gly278ArgfsTer? |