Linked Data
ClinVar Variation Id:
2035385
ClinVar RCV Id:
RCV002877487
MyVariant Identifiers:
chr1:g.216348628G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.216175286G>C , CM000663.2:g.216175286G>C | GRCh38 |
| NC_000001.10:g.216348628G>C , CM000663.1:g.216348628G>C | GRCh37 |
| NC_000001.9:g.214415251G>C | NCBI36 |
| NG_009497.1:g.253111C>G | |
| NG_009497.2:g.253163C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.4593C>G MANE Select | ENSP00000305941.3:p.Pro1531= | |
| ENST00000674083.1:c.4593C>G | ENSP00000501296.1:p.Pro1531= | |
| ENST00000307340.7:c.4593C>G | ENSP00000305941.3:p.Pro1531= | |
| ENST00000366942.3:c.4593C>G | ENSP00000355909.3:p.Pro1531= | |
| NM_007123.5:c.4593C>G | NP_009054.5:p.Pro1531= | |
| NM_206933.2:c.4593C>G | NP_996816.2:p.Pro1531= | |
| NM_206933.3:c.4593C>G | NP_996816.2:p.Pro1531= | |
| NM_007123.6:c.4593C>G | NP_009054.6:p.Pro1531= | |
| NM_206933.4:c.4593C>G MANE Select | NP_996816.3:p.Pro1531= |