Linked Data
gnomAD v4:
10-110577511-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110577511A>T , CM000672.2:g.110577511A>T | GRCh38 |
| NC_000010.10:g.112337269A>T , CM000672.1:g.112337269A>T | GRCh37 |
| NC_000010.9:g.112327259A>T | NCBI36 |
| NG_012217.1:g.14821A>T , LRG_774:g.14821A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.403+19A>T | ||
| ENST00000687823.1:n.184+19A>T | ||
| ENST00000689932.1:n.2333+19A>T | ||
| ENST00000691297.1:n.403+19A>T | ||
| ENST00000691527.1:n.360+19A>T | ||
| ENST00000692792.1:n.389+19A>T | ||
| ENST00000361804.5:c.270+19A>T MANE Select | ENSP00000354720.5:n.270+19A>T | |
| ENST00000361804.4:c.270+19A>T | ENSP00000354720.4:n.270+19A>T | |
| ENST00000462899.1:n.416+19A>T | ||
| NM_005445.3:c.270+19A>T , LRG_774t1:c.270+19A>T | NP_005436.1:n.270+19A>T | |
| NM_005445.4:c.270+19A>T MANE Select | NP_005436.1:n.270+19A>T |