Linked Data
gnomAD v4:
10-110601906-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110601906T>A , CM000672.2:g.110601906T>A | GRCh38 |
| NC_000010.10:g.112361664T>A , CM000672.1:g.112361664T>A | GRCh37 |
| NC_000010.9:g.112351654T>A | NCBI36 |
| NG_012217.1:g.39216T>A , LRG_774:g.39216T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.5125+22T>A | ||
| ENST00000685743.1:n.2600+22T>A | ||
| ENST00000686057.1:n.1243+22T>A | ||
| ENST00000689321.1:n.1855+22T>A | ||
| ENST00000689986.1:n.681+22T>A | ||
| ENST00000361804.5:c.2892+22T>A MANE Select | ENSP00000354720.5:n.2892+22T>A | |
| ENST00000361804.4:c.2892+22T>A | ENSP00000354720.4:n.2892+22T>A | |
| NM_005445.3:c.2892+22T>A , LRG_774t1:c.2892+22T>A | NP_005436.1:n.2892+22T>A | |
| NM_005445.4:c.2892+22T>A MANE Select | NP_005436.1:n.2892+22T>A |