Linked Data
gnomAD v4:
17-42544225-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42544225C>T , CM000679.2:g.42544225C>T | GRCh38 |
| NC_000017.10:g.40696243C>T , CM000679.1:g.40696243C>T | GRCh37 |
| NC_000017.9:g.37949769C>T | NCBI36 |
| NG_011552.1:g.13293C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.2219C>T MANE Select | ENSP00000225927.1:p.Ala740Val | |
| ENST00000225927.6:c.2219C>T | ENSP00000225927.1:p.Ala740Val | |
| NM_000263.3:c.2219C>T | NP_000254.2:p.Ala740Val | |
| XM_006721920.2:c.1388C>T | XP_006721983.1:p.Ala463Val | |
| XM_011524840.1:c.1220C>T | XP_011523142.1:p.Ala407Val | |
| XM_017024687.1:c.1388C>T | XP_016880176.1:p.Ala463Val | |
| XM_024450771.1:c.2276C>T | XP_024306539.1:p.Ala759Val | |
| XM_024450772.1:c.1220C>T | XP_024306540.1:p.Ala407Val | |
| NM_000263.4:c.2219C>T MANE Select | NP_000254.2:p.Ala740Val |