Linked Data
ClinVar Variation Id:
421548
ClinVar RCV Id:
RCV000481984
dbSNP Id:
rs1064795205
gnomAD v3:
12-4379476-C-T
gnomAD v4:
12-4379476-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4379476C>T , CM000674.2:g.4379476C>T | GRCh38 |
| NC_000012.11:g.4488642C>T , CM000674.1:g.4488642C>T | GRCh37 |
| NC_000012.10:g.4358903C>T | NCBI36 |
| NG_007087.1:g.5253G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000237837.2:c.107G>A MANE Select | ENSP00000237837.1:p.Trp36Ter | |
| ENST00000648100.1:c.*1967+13194C>T | ENSP00000497536.1:n.*1967+13194C>T | |
| ENST00000674624.1:c.*1204+13194C>T | ENSP00000501898.1:n.*1204+13194C>T | |
| ENST00000237837.1:c.107G>A | ENSP00000237837.1:p.Trp36Ter | |
| NM_020638.2:c.107G>A | NP_065689.1:p.Trp36Ter | |
| NM_020638.3:c.107G>A MANE Select | NP_065689.1:p.Trp36Ter |