Linked Data
ClinVar Variation Id:
454354
ClinVar RCV Id:
RCV001700199
dbSNP Id:
rs121913634
gnomAD v3:
14-23425372-T-A
gnomAD v4:
14-23425372-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23425372T>A , CM000676.2:g.23425372T>A | GRCh38 |
| NC_000014.8:g.23894581T>A , CM000676.1:g.23894581T>A | GRCh37 |
| NC_000014.7:g.22964421T>A | NCBI36 |
| NG_007884.1:g.15290A>T , LRG_384:g.15290A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000355349.4:c.2333A>T MANE Select | ENSP00000347507.3:p.Asp778Val | |
| ENST00000355349.3:c.2333A>T | ENSP00000347507.3:p.Asp778Val | |
| NM_000257.3:c.2333A>T | NP_000248.2:p.Asp778Val | |
| XR_245686.3:n.2439A>T | ||
| XM_017021340.1:c.2333A>T | XP_016876829.1:p.Asp778Val | |
| NM_000257.4:c.2333A>T MANE Select | NP_000248.2:p.Asp778Val |