Linked Data
ClinVar Variation Id:
2117344
ClinVar RCV Id:
RCV003039155
COSMIC:
COSM4878611
MyVariant Identifiers:
chr22:g.32500781T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32104794T>C , CM000684.2:g.32104794T>C | GRCh38 |
| NC_000022.10:g.32500781T>C , CM000684.1:g.32500781T>C | GRCh37 |
| NC_000022.9:g.30830781T>C | NCBI36 |
| NG_017045.1:g.66763T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266088.9:c.1674T>C MANE Select | ENSP00000266088.4:p.Arg558= | |
| ENST00000266088.8:c.1674T>C | ENSP00000266088.4:p.Arg558= | |
| ENST00000543737.2:c.1293T>C | ENSP00000444898.1:p.Arg431= | |
| NM_000343.3:c.1674T>C | NP_000334.1:p.Arg558= | |
| NM_001256314.1:c.1293T>C | NP_001243243.1:p.Arg431= | |
| XR_938173.1:n.591+2044A>G | ||
| XR_938174.1:n.486+15061A>G | ||
| NM_000343.4:c.1674T>C MANE Select | NP_000334.1:p.Arg558= | |
| NM_001256314.2:c.1293T>C | NP_001243243.1:p.Arg431= |