Linked Data
ClinVar Variation Id:
343804
ClinVar RCV Id:
RCV000368414
dbSNP Id:
rs4680058
ExAC:
3:150645351 G / A
gnomAD v2:
3-150645351-G-A
gnomAD v3:
3-150927564-G-A
gnomAD v4:
3-150927564-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.150927564G>A , CM000665.2:g.150927564G>A | GRCh38 |
| NC_000003.11:g.150645351G>A , CM000665.1:g.150645351G>A | GRCh37 |
| NC_000003.10:g.152128041G>A | NCBI36 |
| NG_009168.1:g.50436C>T , LRG_700:g.50436C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000327047.6:c.*372C>T MANE Select | ENSP00000322280.1:n.*372C>T | |
| ENST00000295911.6:c.342+501C>T | ENSP00000295911.2:n.342+501C>T | |
| ENST00000327047.5:c.*372C>T | ENSP00000322280.1:n.*372C>T | |
| ENST00000562308.5:c.104+14018C>T | ||
| ENST00000565169.1:c.162+14018C>T | ||
| ENST00000569170.5:c.162+14018C>T | ||
| NM_001195794.1:c.*372C>T , LRG_700t1:c.*372C>T | NP_001182723.1:n.*372C>T | |
| NM_001256819.1:c.*685C>T | NP_001243748.1:n.*685C>T | |
| NM_052995.2:c.342+501C>T , LRG_700t2:c.342+501C>T | NP_443721.1:n.342+501C>T | |
| NM_174878.2:c.*372C>T | NP_777367.1:n.*372C>T | |
| NR_046380.2:n.1552C>T | ||
| XR_924167.1:n.1383C>T | ||
| NM_001256819.2:c.*685C>T | NP_001243748.1:n.*685C>T | |
| NM_174878.3:c.*372C>T MANE Select | NP_777367.1:n.*372C>T | |
| NR_046380.3:n.1280C>T |