Linked Data
ClinVar Variation Id:
393061
ClinVar RCV Id:
RCV000425453
dbSNP Id:
rs1057524766
gnomAD v4:
1-2228739-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.2228739G>T , CM000663.2:g.2228739G>T | GRCh38 |
| NC_000001.10:g.2160178G>T , CM000663.1:g.2160178G>T | GRCh37 |
| NC_000001.9:g.2150038G>T | NCBI36 |
| NG_013084.1:g.5045G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000704337.1:n.137+1215G>T | ||
| ENST00000378536.5:c.-28G>T MANE Select | ENSP00000367797.4:n.-28G>T | |
| ENST00000378536.4:c.-28G>T | ENSP00000367797.4:n.-28G>T | |
| NM_003036.3:c.-28G>T | NP_003027.1:n.-28G>T | |
| XM_005244775.2:c.-28G>T | XP_005244832.1:n.-28G>T | |
| XM_005244775.3:c.-28G>T | XP_005244832.1:n.-28G>T | |
| NM_003036.4:c.-28G>T MANE Select | NP_003027.1:n.-28G>T |