Linked Data
ClinVar Variation Id:
13075
dbSNP Id:
rs587776782
gnomAD v4:
13-48367604-G-T
COSMIC:
COSM1041
PubMed:
PMID:2594029
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48367604G>T , CM000675.2:g.48367604G>T | GRCh38 |
| NC_000013.10:g.48941740G>T , CM000675.1:g.48941740G>T | GRCh37 |
| NC_000013.9:g.47839741G>T | NCBI36 |
| NG_009009.1:g.68858G>T , LRG_517:g.68858G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.1049+1G>T MANE Select | ENSP00000267163.4:n.1049+1G>T | |
| ENST00000650461.1:c.1049+1G>T | ENSP00000497193.1:n.1049+1G>T | |
| ENST00000267163.4:c.1049+1G>T | ENSP00000267163.4:n.1049+1G>T | |
| NM_000321.2:c.1049+1G>T , LRG_517t1:c.1049+1G>T | NP_000312.2:n.1049+1G>T | |
| XM_011535171.1:c.788+1G>T | XP_011533473.1:n.788+1G>T | |
| XM_011535171.2:c.788+1G>T | XP_011533473.1:n.788+1G>T | |
| XR_002957522.1:n.122-2628C>A | ||
| NM_000321.3:c.1049+1G>T MANE Select | NP_000312.2:n.1049+1G>T |