Linked Data
gnomAD v4:
20-44651879-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.44651879C>A , CM000682.2:g.44651879C>A | GRCh38 |
| NC_000020.10:g.43280520C>A , CM000682.1:g.43280520C>A | GRCh37 |
| NC_000020.9:g.42713934C>A | NCBI36 |
| NG_007385.1:g.4857G>T , LRG_16:g.4857G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000536076.2:c.-121+23G>T | ENSP00000512234.1:n.-121+23G>T | |
| ENST00000696039.1:n.321+23G>T | ||
| ENST00000696062.1:c.96+221G>T | ENSP00000512365.1:n.96+221G>T | |
| ENST00000696064.1:c.-118+23G>T | ENSP00000512367.1:n.-118+23G>T | |
| ENST00000696065.1:c.-121+23G>T | ENSP00000512368.1:n.-121+23G>T | |
| ENST00000535573.1:n.332+23G>T | ||
| ENST00000536076.1:n.213+23G>T | ||
| XM_011528479.1:c.-257+23G>T | XP_011526781.1:n.-257+23G>T |