Linked Data
gnomAD v4:
21-43776266-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.43776266T>A , CM000683.2:g.43776266T>A | GRCh38 |
| NC_000021.8:g.45196147T>A , CM000683.1:g.45196147T>A | GRCh37 |
| NC_000021.7:g.44020575T>A | NCBI36 |
| NG_011545.1:g.5113A>T , LRG_485:g.5113A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291568.7:c.4A>T MANE Select | ENSP00000291568.6:p.Met2Leu | |
| ENST00000480147.3:n.3A>T | ||
| ENST00000640406.1:c.4A>T | ENSP00000492672.1:p.Met2Leu | |
| ENST00000675996.1:n.65A>T | ||
| ENST00000291568.5:c.4A>T | ENSP00000291568.5:p.Met2Leu | |
| ENST00000480147.1:n.41A>T | ||
| NM_000100.3:c.4A>T , LRG_485t1:c.4A>T | NP_000091.1:p.Met2Leu | |
| NM_000100.4:c.4A>T MANE Select | NP_000091.1:p.Met2Leu |