Linked Data
gnomAD v4:
10-14436436-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.14436436C>A , CM000672.2:g.14436436C>A | GRCh38 |
| NC_000010.10:g.14478435C>A , CM000672.1:g.14478435C>A | GRCh37 |
| NC_000010.9:g.14518441C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000475141.2:c.-305+25632G>T | ENSP00000473870.1:n.-305+25632G>T | |
| ENST00000493380.5:c.-82+25632G>T | ENSP00000474863.1:n.-82+25632G>T |