Linked Data
ClinVar Variation Id:
48276
ClinVar RCV Id:
RCV000041590
dbSNP Id:
rs111033447
gnomAD v3:
2-26495011-G-T
gnomAD v4:
2-26495011-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.26495011G>T , CM000664.2:g.26495011G>T | GRCh38 |
| NC_000002.11:g.26717879G>T , CM000664.1:g.26717879G>T | GRCh37 |
| NC_000002.10:g.26571383G>T | NCBI36 |
| NG_009937.1:g.68688C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000272371.7:c.828C>A MANE Select | ENSP00000272371.2:p.Cys276Ter | |
| ENST00000272371.6:c.828C>A | ENSP00000272371.2:p.Cys276Ter | |
| ENST00000403946.7:c.828C>A | ENSP00000385255.3:p.Cys276Ter | |
| NM_001287489.1:c.828C>A | NP_001274418.1:p.Cys276Ter | |
| NM_194248.2:c.828C>A | NP_919224.1:p.Cys276Ter | |
| XM_005264644.2:c.873C>A | XP_005264701.1:p.Cys291Ter | |
| XM_011533185.1:c.873C>A | XP_011531487.1:p.Cys291Ter | |
| XM_017005338.1:c.828C>A | XP_016860827.1:p.Cys276Ter | |
| NM_001287489.2:c.828C>A | NP_001274418.1:p.Cys276Ter | |
| NM_194248.3:c.828C>A MANE Select | NP_919224.1:p.Cys276Ter |