Linked Data
dbSNP Id:
rs148771817
gnomAD v2:
7-120742980-C-T
gnomAD v3:
7-121102926-C-T
gnomAD v4:
7-121102926-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.121102926C>T , CM000669.2:g.121102926C>T | GRCh38 |
| NC_000007.13:g.120742980C>T , CM000669.1:g.120742980C>T | GRCh37 |
| NC_000007.12:g.120530216C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000310396.10:c.918+2832C>T MANE Select | ENSP00000309772.5:n.918+2832C>T | |
| ENST00000310396.9:c.918+2832C>T | ENSP00000309772.5:n.918+2832C>T | |
| ENST00000423795.5:c.258+2832C>T | ENSP00000415573.1:n.258+2832C>T | |
| ENST00000428526.5:c.918+2832C>T | ENSP00000398082.1:n.918+2832C>T | |
| ENST00000443817.1:c.258+2832C>T | ENSP00000391952.1:n.258+2832C>T | |
| ENST00000450913.6:c.918+2832C>T | ENSP00000406122.2:n.918+2832C>T | |
| NM_001105533.1:c.918+2832C>T | NP_001099003.1:n.918+2832C>T | |
| NM_024913.4:c.918+2832C>T | NP_079189.4:n.918+2832C>T | |
| XM_011516583.1:c.918+2832C>T | XP_011514885.1:n.918+2832C>T | |
| XM_017012649.2:c.918+2832C>T | XP_016868138.1:n.918+2832C>T | |
| XM_024446941.1:c.405+2832C>T | XP_024302709.1:n.405+2832C>T | |
| NM_024913.5:c.918+2832C>T MANE Select | NP_079189.4:n.918+2832C>T |