Linked Data
ClinVar Variation Id:
2453252
ClinVar RCV Id:
RCV003182707
dbSNP Id:
rs1759497850
MyVariant Identifiers:
chr6:g.7583297A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.7583064A>G , CM000668.2:g.7583064A>G | GRCh38 |
| NC_000006.11:g.7583297A>G , CM000668.1:g.7583297A>G | GRCh37 |
| NC_000006.10:g.7528296A>G | NCBI36 |
| NG_008803.1:g.46428A>G , LRG_423:g.46428A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710359.1:c.4473A>G | ENSP00000518230.1:p.Arg1491= | |
| ENST00000379802.8:c.5802A>G MANE Select | ENSP00000369129.3:p.Arg1934= | |
| ENST00000379802.7:c.5802A>G | ENSP00000369129.3:p.Arg1934= | |
| ENST00000418664.2:c.4005A>G | ENSP00000396591.2:p.Arg1335= | |
| NM_001008844.1:c.4005A>G | NP_001008844.1:p.Arg1335= | |
| NM_004415.2:c.5802A>G , LRG_423t1:c.5802A>G | NP_004406.2:p.Arg1934= | |
| XM_011514323.1:c.4473A>G | XP_011512625.1:p.Arg1491= | |
| NM_001008844.2:c.4005A>G | NP_001008844.1:p.Arg1335= | |
| NM_001319034.1:c.4473A>G | NP_001305963.1:p.Arg1491= | |
| NM_004415.3:c.5802A>G | NP_004406.2:p.Arg1934= | |
| NM_004415.4:c.5802A>G MANE Select | NP_004406.2:p.Arg1934= | |
| NM_001008844.3:c.4005A>G | NP_001008844.1:p.Arg1335= | |
| NM_001319034.2:c.4473A>G | NP_001305963.1:p.Arg1491= |