Linked Data
ClinVar Variation Id:
1034649
ClinVar RCV Id:
RCV001337406
dbSNP Id:
rs878854579
COSMIC:
COSM5613817
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17022663G>A , CM000663.2:g.17022663G>A | GRCh38 |
| NC_000001.10:g.17349158G>A , CM000663.1:g.17349158G>A | GRCh37 |
| NC_000001.9:g.17221745G>A | NCBI36 |
| NG_012340.1:g.36508C>T , LRG_316:g.36508C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463045.3:c.539C>T | ENSP00000481376.2:p.Pro180Leu | |
| ENST00000491274.6:c.668C>T | ENSP00000480482.2:p.Pro223Leu | |
| ENST00000375499.8:c.710C>T MANE Select | ENSP00000364649.3:p.Pro237Leu | |
| ENST00000375499.7:c.710C>T | ENSP00000364649.3:p.Pro237Leu | |
| ENST00000475049.5:n.135C>T | ||
| ENST00000485092.5:n.374C>T | ||
| ENST00000485515.5:n.644C>T | ||
| NM_003000.2:c.710C>T , LRG_316t1:c.710C>T | NP_002991.2:p.Pro237Leu | |
| NM_003000.3:c.710C>T MANE Select | NP_002991.2:p.Pro237Leu |