Linked Data
ClinVar Variation Id:
2812123
ClinVar RCV Id:
RCV003685257
MyVariant Identifiers:
chr6:g.64940588T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.64230695T>C , CM000668.2:g.64230695T>C | GRCh38 |
| NC_000006.11:g.64940588T>C , CM000668.1:g.64940588T>C | GRCh37 |
| NC_000006.10:g.64998547T>C | NCBI36 |
| NG_023443.1:g.1481531A>G | |
| NG_023443.2:g.1481531A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000503581.6:c.6321A>G MANE Select | ENSP00000424243.1:p.Val2107= | |
| ENST00000370616.6:c.6321A>G | ENSP00000359650.2:p.Val2107= | |
| ENST00000370618.7:c.6321A>G | ENSP00000359652.4:p.Val2107= | |
| ENST00000370621.7:c.6321A>G | ENSP00000359655.3:p.Val2107= | |
| ENST00000503581.5:c.6321A>G | ENSP00000424243.1:p.Val2107= | |
| NM_001142800.1:c.6321A>G | NP_001136272.1:p.Val2107= | |
| NM_001292009.1:c.6321A>G | NP_001278938.1:p.Val2107= | |
| NM_001142800.2:c.6321A>G MANE Select | NP_001136272.1:p.Val2107= | |
| NM_001292009.2:c.6321A>G | NP_001278938.1:p.Val2107= |