Linked Data
gnomAD v4:
3-138945879-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.138945879C>T , CM000665.2:g.138945879C>T | GRCh38 |
| NC_000003.11:g.138664721C>T , CM000665.1:g.138664721C>T | GRCh37 |
| NC_000003.10:g.140147411C>T | NCBI36 |
| NG_012454.1:g.6262G>A | |
| NG_029796.1:g.3646C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648323.1:c.844G>A MANE Select | ENSP00000497217.1:p.Ala282Thr | |
| ENST00000330315.3:c.844G>A | ENSP00000333188.3:p.Ala282Thr | |
| NM_023067.3:c.844G>A | NP_075555.1:p.Ala282Thr | |
| NM_023067.4:c.844G>A MANE Select | NP_075555.1:p.Ala282Thr |