Linked Data
gnomAD v4:
21-34370413-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.34370413A>T , CM000683.2:g.34370413A>T | GRCh38 |
| NC_000021.8:g.35742712A>T , CM000683.1:g.35742712A>T | GRCh37 |
| NC_000021.7:g.34664582A>T | NCBI36 |
| NG_008804.1:g.11390A>T , LRG_291:g.11390A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000290310.4:c.-12-54A>T MANE Select | ENSP00000290310.2:n.-12-54A>T | |
| ENST00000290310.3:c.-12-54A>T | ENSP00000290310.2:n.-12-54A>T | |
| NM_172201.1:c.-12-54A>T , LRG_291t1:c.-12-54A>T | NP_751951.1:n.-12-54A>T | |
| XR_937683.1:n.886+22T>A | ||
| XR_937684.1:n.886+22T>A | ||
| XR_001755012.2:n.1029T>A | ||
| XR_001755013.2:n.908T>A | ||
| XR_937683.2:n.886+22T>A | ||
| NM_172201.2:c.-12-54A>T MANE Select | NP_751951.1:n.-12-54A>T |