Linked Data
gnomAD v4:
21-43776223-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.43776223G>T , CM000683.2:g.43776223G>T | GRCh38 |
| NC_000021.8:g.45196104G>T , CM000683.1:g.45196104G>T | GRCh37 |
| NC_000021.7:g.44020532G>T | NCBI36 |
| NG_011545.1:g.5156C>A , LRG_485:g.5156C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291568.7:c.47C>A MANE Select | ENSP00000291568.6:p.Thr16Asn | |
| ENST00000480147.3:n.46C>A | ||
| ENST00000639959.1:c.16C>A | ||
| ENST00000640406.1:c.47C>A | ENSP00000492672.1:p.Thr16Asn | |
| ENST00000675996.1:n.108C>A | ||
| ENST00000291568.5:c.47C>A | ENSP00000291568.5:p.Thr16Asn | |
| ENST00000480147.1:n.84C>A | ||
| NM_000100.3:c.47C>A , LRG_485t1:c.47C>A | NP_000091.1:p.Thr16Asn | |
| NM_000100.4:c.47C>A MANE Select | NP_000091.1:p.Thr16Asn |