Linked Data
gnomAD v4:
5-53560634-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.53560634C>A , CM000667.2:g.53560634C>A | GRCh38 |
| NC_000005.9:g.52856464C>A , CM000667.1:g.52856464C>A | GRCh37 |
| NC_000005.8:g.52892221C>A | NCBI36 |
| NG_008200.1:g.5000C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000507026.5:c.-29C>A | ENSP00000424993.1:n.-29C>A | |
| XM_005248525.3:c.-29C>A | XP_005248582.1:n.-29C>A | |
| XM_011543414.1:c.-29C>A | XP_011541716.1:n.-29C>A | |
| NM_001318051.1:c.-29C>A | NP_001304980.1:n.-29C>A | |
| NM_002495.3:c.-29C>A | NP_002486.1:n.-29C>A | |
| NR_134473.1:n.2C>A | ||
| NR_134474.1:n.2C>A | ||
| NR_134475.1:n.2C>A | ||
| XM_017009491.1:c.-29C>A | XP_016864980.1:n.-29C>A |