Linked Data
ClinVar Variation Id:
626145
ClinVar RCV Id:
RCV000768278
dbSNP Id:
rs1060502176
COSMIC:
COSM6188362
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.100407891G>A , CM000685.2:g.100407891G>A | GRCh38 |
| NC_000023.10:g.99662889G>A , CM000685.1:g.99662889G>A | GRCh37 |
| NC_000023.9:g.99549545G>A | NCBI36 |
| NG_021319.1:g.7383C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000255531.8:c.707C>T | ENSP00000255531.7:p.Pro236Leu | |
| ENST00000373034.8:c.707C>T MANE Select | ENSP00000362125.4:p.Pro236Leu | |
| ENST00000420881.6:c.707C>T | ENSP00000400327.2:p.Pro236Leu | |
| NM_001105243.1:c.707C>T | NP_001098713.1:p.Pro236Leu | |
| NM_001184880.1:c.707C>T | NP_001171809.1:p.Pro236Leu | |
| NM_020766.2:c.707C>T | NP_065817.2:p.Pro236Leu | |
| XM_011530997.1:c.707C>T | XP_011529299.1:p.Pro236Leu | |
| XM_011530997.2:c.707C>T | XP_011529299.1:p.Pro236Leu | |
| NM_001105243.2:c.707C>T | NP_001098713.1:p.Pro236Leu | |
| NM_001184880.2:c.707C>T MANE Select | NP_001171809.1:p.Pro236Leu | |
| NM_020766.3:c.707C>T | NP_065817.2:p.Pro236Leu |