Linked Data
ClinVar Variation Id:
1653211
ClinVar RCV Id:
RCV002160948
dbSNP Id:
rs2101644408
MyVariant Identifiers:
chr1:g.55464925T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.54999252T>C , CM000663.2:g.54999252T>C | GRCh38 |
| NC_000001.10:g.55464925T>C , CM000663.1:g.55464925T>C | GRCh37 |
| NC_000001.9:g.55237513T>C | NCBI36 |
| NG_008965.1:g.5309T>C | |
| NG_008965.2:g.5320T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651561.1:c.66T>C MANE Select | ENSP00000498282.1:p.Gly22= | |
| ENST00000371265.4:c.66T>C | ENSP00000360312.4:p.Gly22= | |
| NM_057176.2:c.66T>C | NP_476517.1:p.Gly22= | |
| NM_057176.3:c.66T>C MANE Select | NP_476517.1:p.Gly22= |