Linked Data
gnomAD v4:
1-15445732-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.15445732A>T , CM000663.2:g.15445732A>T | GRCh38 |
| NC_000001.10:g.15772227A>T , CM000663.1:g.15772227A>T | GRCh37 |
| NC_000001.9:g.15644814A>T | NCBI36 |
| NG_009253.1:g.12290A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375949.5:c.775A>T MANE Select | ENSP00000365116.4:p.Ile259Phe | |
| ENST00000375943.6:c.*229A>T | ENSP00000365110.2:n.*229A>T | |
| ENST00000375949.4:c.775A>T | ENSP00000365116.4:p.Ile259Phe | |
| ENST00000483406.1:n.539A>T | ||
| NM_007272.2:c.775A>T | NP_009203.2:p.Ile259Phe | |
| XM_011540550.1:c.629A>T | XP_011538852.1:p.His210Leu | |
| NM_007272.3:c.775A>T MANE Select | NP_009203.2:p.Ile259Phe |