Linked Data
ClinVar Variation Id:
2918761
ClinVar RCV Id:
RCV003609965
dbSNP Id:
rs777398890
ExAC:
12:124228803 C / T
gnomAD v2:
12-124228803-C-T
gnomAD v4:
12-123744256-C-T
COSMIC:
COSM2226085
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.123744256C>T , CM000674.2:g.123744256C>T | GRCh38 |
| NC_000012.11:g.124228803C>T , CM000674.1:g.124228803C>T | GRCh37 |
| NC_000012.10:g.122794756C>T | NCBI36 |
| NG_012743.1:g.36939C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330342.8:c.1245C>T MANE Select | ENSP00000332247.2:p.Phe415= | |
| ENST00000540368.6:n.1276C>T | ||
| ENST00000674794.1:c.1333C>T | ||
| ENST00000675260.1:n.520C>T | ||
| ENST00000675344.1:c.*266C>T | ENSP00000501953.1:n.*266C>T | |
| ENST00000330342.7:c.1245C>T | ENSP00000332247.2:p.Phe415= | |
| ENST00000504192.2:c.855C>T | ENSP00000443441.1:p.Phe285= | |
| ENST00000536426.1:n.262C>T | ||
| ENST00000545059.5:n.3881C>T | ||
| NM_012463.3:c.1245C>T | NP_036595.2:p.Phe415= | |
| XM_005253563.1:c.1245C>T | XP_005253620.1:p.Phe415= | |
| XM_006719317.2:c.732C>T | XP_006719380.1:p.Phe244= | |
| XM_006719318.2:c.423C>T | XP_006719381.1:p.Phe141= | |
| XR_429088.1:n.1408C>T | ||
| XM_024448910.1:c.1245C>T | XP_024304678.1:p.Phe415= | |
| XM_024448911.1:c.732C>T | XP_024304679.1:p.Phe244= | |
| XM_024448912.1:c.423C>T | XP_024304680.1:p.Phe141= | |
| NM_012463.4:c.1245C>T MANE Select | NP_036595.2:p.Phe415= |