Linked Data
ClinVar Variation Id:
2922953
ClinVar RCV Id:
RCV003788119
dbSNP Id:
rs1308974655
gnomAD v2:
1-43803755-C-T
gnomAD v4:
1-43338084-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.43338084C>T , CM000663.2:g.43338084C>T | GRCh38 |
| NC_000001.10:g.43803755C>T , CM000663.1:g.43803755C>T | GRCh37 |
| NC_000001.9:g.43576342C>T | NCBI36 |
| NG_007525.1:g.5281C>T , LRG_510:g.5281C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372470.9:c.80-15C>T MANE Select | ENSP00000361548.3:n.80-15C>T | |
| ENST00000413998.7:c.80-36C>T | ENSP00000414004.3:n.80-36C>T | |
| ENST00000638732.1:n.80-15C>T | ||
| ENST00000372470.7:c.80-15C>T | ENSP00000361548.3:n.80-15C>T | |
| ENST00000413998.6:c.80-15C>T | ENSP00000414004.2:n.80-15C>T | |
| ENST00000612993.1:c.80-15C>T | ENSP00000480273.1:n.80-15C>T | |
| NM_005373.2:c.80-15C>T , LRG_510t1:c.80-15C>T | NP_005364.1:n.80-15C>T | |
| XM_011541478.1:c.80-36C>T | XP_011539780.1:n.80-36C>T | |
| XM_017001320.1:c.236C>T | XP_016856809.1:p.Thr79Ile | |
| NM_005373.3:c.80-15C>T MANE Select | NP_005364.1:n.80-15C>T |