Linked Data
gnomAD v4:
10-110573758-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110573758T>C , CM000672.2:g.110573758T>C | GRCh38 |
| NC_000010.10:g.112333516T>C , CM000672.1:g.112333516T>C | GRCh37 |
| NC_000010.9:g.112323506T>C | NCBI36 |
| NG_012217.1:g.11068T>C , LRG_774:g.11068T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.263+13T>C | ||
| ENST00000687823.1:n.45-1578T>C | ||
| ENST00000689932.1:n.616T>C | ||
| ENST00000691297.1:n.263+13T>C | ||
| ENST00000691527.1:n.220+13T>C | ||
| ENST00000692792.1:n.249+13T>C | ||
| ENST00000361804.5:c.130+13T>C MANE Select | ENSP00000354720.5:n.130+13T>C | |
| ENST00000361804.4:c.130+13T>C | ENSP00000354720.4:n.130+13T>C | |
| ENST00000462899.1:n.276+13T>C | ||
| NM_005445.3:c.130+13T>C , LRG_774t1:c.130+13T>C | NP_005436.1:n.130+13T>C | |
| NM_005445.4:c.130+13T>C MANE Select | NP_005436.1:n.130+13T>C |