Linked Data
gnomAD v4:
7-255761-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.255761A>T , CM000669.2:g.255761A>T | GRCh38 |
| NC_000007.13:g.295727A>T , CM000669.1:g.295727A>T | GRCh37 |
| NG_033970.1:g.65397A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000313766.6:c.1073-88A>T MANE Select | ENSP00000322323.5:n.1073-88A>T | |
| ENST00000313766.5:c.1073-88A>T | ENSP00000322323.5:n.1073-88A>T | |
| ENST00000515795.1:n.730-88A>T | ||
| NM_020223.3:c.1073-88A>T | NP_064608.2:n.1073-88A>T | |
| XR_242097.3:n.1220-88A>T | ||
| XM_017012450.1:c.1334-88A>T | XP_016867939.1:n.1334-88A>T | |
| XM_017012451.1:c.1331-88A>T | XP_016867940.1:n.1331-88A>T | |
| XM_017012455.2:c.371-88A>T | XP_016867944.1:n.371-88A>T | |
| NM_020223.4:c.1073-88A>T MANE Select | NP_064608.2:n.1073-88A>T |