Linked Data
ClinVar Variation Id:
1575850
ClinVar RCV Id:
RCV002093003
dbSNP Id:
rs778384637
ExAC:
19:1495501 C / T
gnomAD v2:
19-1495501-C-T
gnomAD v3:
19-1495502-C-T
gnomAD v4:
19-1495502-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1495502C>T , CM000681.2:g.1495502C>T | GRCh38 |
| NC_000019.9:g.1495501C>T , CM000681.1:g.1495501C>T | GRCh37 |
| NC_000019.8:g.1446501C>T | NCBI36 |
| NG_055254.1:g.9498C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233596.8:c.243C>T MANE Select | ENSP00000233596.2:p.Asp81= | |
| ENST00000395479.10:c.243C>T MANE Plus Clinical | ENSP00000378861.5:p.Asp81= | |
| ENST00000233596.7:c.243C>T | ENSP00000233596.2:p.Asp81= | |
| ENST00000395479.8:c.59C>T | ||
| ENST00000395484.4:c.27C>T | ENSP00000378865.4:p.Asp9= | |
| ENST00000591735.2:n.347C>T | ||
| NM_138393.1:c.243C>T | NP_612402.1:p.Asp81= | |
| NM_001329556.2:c.243C>T | NP_001316485.1:p.Asp81= | |
| NM_138393.3:c.243C>T | NP_612402.1:p.Asp81= | |
| NM_138393.4:c.243C>T MANE Select | NP_612402.1:p.Asp81= | |
| NM_001329556.3:c.243C>T MANE Plus Clinical | NP_001316485.1:p.Asp81= |