Linked Data
ClinVar Variation Id:
1034637
ClinVar RCV Id:
RCV001337391
dbSNP Id:
rs1172777549
gnomAD v2:
12-5154199-C-T
gnomAD v3:
12-5045033-C-T
gnomAD v4:
12-5045033-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5045033C>T , CM000674.2:g.5045033C>T | GRCh38 |
| NC_000012.11:g.5154199C>T , CM000674.1:g.5154199C>T | GRCh37 |
| NC_000012.10:g.5024460C>T | NCBI36 |
| NG_012198.1:g.6115C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252321.5:c.886C>T MANE Select | ENSP00000252321.3:p.Pro296Ser | |
| ENST00000252321.4:c.886C>T | ENSP00000252321.3:p.Pro296Ser | |
| NM_002234.3:c.886C>T | NP_002225.2:p.Pro296Ser | |
| NM_002234.4:c.886C>T MANE Select | NP_002225.2:p.Pro296Ser |