Linked Data
gnomAD v4:
10-110575358-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110575358T>A , CM000672.2:g.110575358T>A | GRCh38 |
| NC_000010.10:g.112335116T>A , CM000672.1:g.112335116T>A | GRCh37 |
| NC_000010.9:g.112325106T>A | NCBI36 |
| NG_012217.1:g.12668T>A , LRG_774:g.12668T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.286T>A | ||
| ENST00000687823.1:n.67T>A | ||
| ENST00000689932.1:n.2216T>A | ||
| ENST00000691297.1:n.286T>A | ||
| ENST00000691527.1:n.243T>A | ||
| ENST00000692792.1:n.272T>A | ||
| ENST00000361804.5:c.153T>A MANE Select | ENSP00000354720.5:p.Asp51Glu | |
| ENST00000361804.4:c.153T>A | ENSP00000354720.4:p.Asp51Glu | |
| ENST00000462899.1:n.299T>A | ||
| NM_005445.3:c.153T>A , LRG_774t1:c.153T>A | NP_005436.1:p.Asp51Glu | |
| NM_005445.4:c.153T>A MANE Select | NP_005436.1:p.Asp51Glu |