Linked Data
ClinVar Variation Id:
2921203
ClinVar RCV Id:
RCV003740621
dbSNP Id:
rs1323375123
gnomAD v2:
18-29172874-A-T
gnomAD v4:
18-31592911-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31592911A>T , CM000680.2:g.31592911A>T | GRCh38 |
| NC_000018.9:g.29172874A>T , CM000680.1:g.29172874A>T | GRCh37 |
| NC_000018.8:g.27426872A>T | NCBI36 |
| NG_009490.1:g.6145A>T , LRG_416:g.6145A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000237014.8:c.85A>T MANE Select | ENSP00000237014.4:p.Lys29Ter | |
| ENST00000610404.5:c.-12A>T | ENSP00000477599.2:n.-12A>T | |
| ENST00000649620.1:c.85A>T | ENSP00000497927.1:p.Lys29Ter | |
| ENST00000237014.7:c.85A>T | ENSP00000237014.3:p.Lys29Ter | |
| ENST00000432547.7:n.111A>T | ||
| ENST00000541025.2:n.111A>T | ||
| ENST00000610404.4:c.85A>T | ENSP00000477599.1:p.Lys29Ter | |
| ENST00000613781.1:c.85A>T | ENSP00000479174.1:p.Lys29Ter | |
| NM_000371.3:c.85A>T , LRG_416t1:c.85A>T | NP_000362.1:p.Lys29Ter | |
| NM_000371.4:c.85A>T MANE Select | NP_000362.1:p.Lys29Ter |