Linked Data
ClinVar Variation Id:
753310
ClinVar RCV Id:
RCV001424302
dbSNP Id:
rs1388869180
gnomAD v3:
2-202542457-A-T
gnomAD v4:
2-202542457-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202542457A>T , CM000664.2:g.202542457A>T | GRCh38 |
| NC_000002.11:g.203407180A>T , CM000664.1:g.203407180A>T | GRCh37 |
| NC_000002.10:g.203115425A>T | NCBI36 |
| NG_009363.1:g.171131A>T , LRG_712:g.171131A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374580.10:c.1413+10A>T MANE Select | ENSP00000363708.4:n.1413+10A>T | |
| ENST00000638587.1:c.1344+10A>T | ENSP00000491062.1:n.1344+10A>T | |
| ENST00000374574.2:c.1413+10A>T | ENSP00000363702.2:n.1413+10A>T | |
| ENST00000374580.8:c.1413+10A>T | ENSP00000363708.4:n.1413+10A>T | |
| NM_001204.6:c.1413+10A>T , LRG_712t1:c.1413+10A>T | NP_001195.2:n.1413+10A>T | |
| XM_011511687.1:c.1413+10A>T | XP_011509989.1:n.1413+10A>T | |
| XM_011511688.1:c.1413+10A>T | XP_011509990.1:n.1413+10A>T | |
| NM_001204.7:c.1413+10A>T MANE Select | NP_001195.2:n.1413+10A>T |