Linked Data
gnomAD v4:
20-44118416-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.44118416A>T , CM000682.2:g.44118416A>T | GRCh38 |
| NC_000020.10:g.42747056A>T , CM000682.1:g.42747056A>T | GRCh37 |
| NC_000020.9:g.42180470A>T | NCBI36 |
| NG_031867.1:g.74163T>A , LRG_394:g.74163T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372980.4:c.1288+89T>A MANE Select | ENSP00000362071.3:n.1288+89T>A | |
| ENST00000372980.3:c.1288+89T>A | ENSP00000362071.3:n.1288+89T>A | |
| NM_020433.4:c.1288+89T>A , LRG_394t1:c.1288+89T>A | NP_065166.2:n.1288+89T>A | |
| XM_006723832.2:c.1288+89T>A | XP_006723895.1:n.1288+89T>A | |
| NM_020433.5:c.1288+89T>A MANE Select | NP_065166.2:n.1288+89T>A |