Linked Data
ClinVar Variation Id:
1136230
ClinVar RCV Id:
RCV001471795
dbSNP Id:
rs762224660
MyVariant Identifiers:
chr17:g.37821645G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39665392G>T , CM000679.2:g.39665392G>T | GRCh38 |
| NC_000017.10:g.37821645G>T , CM000679.1:g.37821645G>T | GRCh37 |
| NC_000017.9:g.35075171G>T | NCBI36 |
| NG_008892.1:g.5047G>T , LRG_210:g.5047G>T | |
| NG_042278.1:g.2412G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309889.3:c.33G>T MANE Select | ENSP00000312624.2:p.Ser11= | |
| ENST00000309889.2:c.33G>T | ENSP00000312624.2:p.Ser11= | |
| ENST00000578283.1:c.33G>T | ENSP00000462787.1:p.Ser11= | |
| NM_003673.3:c.33G>T , LRG_210t1:c.33G>T | NP_003664.1:p.Ser11= | |
| NM_003673.4:c.33G>T MANE Select | NP_003664.1:p.Ser11= |