Linked Data
ClinVar Variation Id:
1782843
ClinVar RCV Id:
RCV002410876
dbSNP Id:
rs1837617736
gnomAD v4:
10-43100577-C-T
MyVariant Identifiers:
chr10:g.43596025C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.43100577C>T , CM000672.2:g.43100577C>T | GRCh38 |
| NC_000010.10:g.43596025C>T , CM000672.1:g.43596025C>T | GRCh37 |
| NC_000010.9:g.42916031C>T | NCBI36 |
| NG_007489.1:g.28509C>T , LRG_518:g.28509C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000615310.5:c.192C>T | ENSP00000480088.2:p.Pro64= | |
| ENST00000683278.1:c.94C>T | ||
| ENST00000684216.1:c.94C>T | ||
| ENST00000340058.6:c.192C>T | ENSP00000344798.4:p.Pro64= | |
| ENST00000355710.8:c.192C>T MANE Select | ENSP00000347942.3:p.Pro64= | |
| ENST00000638465.1:c.94C>T | ||
| ENST00000640619.1:c.94C>T | ||
| ENST00000671844.1:c.192C>T | ENSP00000500541.1:p.Pro64= | |
| ENST00000672389.1:c.74-10630C>T | ENSP00000500252.1:n.74-10630C>T | |
| ENST00000340058.5:c.192C>T | ENSP00000344798.4:p.Pro64= | |
| ENST00000355710.7:c.192C>T | ENSP00000347942.3:p.Pro64= | |
| ENST00000498820.5:c.74-11522C>T | ENSP00000419080.1:n.74-11522C>T | |
| ENST00000615310.4:c.192C>T | ENSP00000480088.1:p.Pro64= | |
| NM_020630.4:c.192C>T , LRG_518t2:c.192C>T | NP_065681.1:p.Pro64= | |
| NM_020975.4:c.192C>T , LRG_518t1:c.192C>T | NP_066124.1:p.Pro64= | |
| XM_011540027.1:c.192C>T | XP_011538329.1:p.Pro64= | |
| NM_020630.5:c.192C>T | NP_065681.1:p.Pro64= | |
| NM_020975.5:c.192C>T | NP_066124.1:p.Pro64= | |
| NM_020975.6:c.192C>T MANE Select | NP_066124.1:p.Pro64= | |
| NM_020630.6:c.192C>T | NP_065681.1:p.Pro64= |