Linked Data
ClinVar Variation Id:
2940843
ClinVar RCV Id:
RCV003792105
MyVariant Identifiers:
chr6:g.7585442G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.7585209G>A , CM000668.2:g.7585209G>A | GRCh38 |
| NC_000006.11:g.7585442G>A , CM000668.1:g.7585442G>A | GRCh37 |
| NC_000006.10:g.7530441G>A | NCBI36 |
| NG_008803.1:g.48573G>A , LRG_423:g.48573G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710359.1:c.6618G>A | ENSP00000518230.1:p.Arg2206= | |
| ENST00000379802.8:c.7947G>A MANE Select | ENSP00000369129.3:p.Arg2649= | |
| ENST00000379802.7:c.7947G>A | ENSP00000369129.3:p.Arg2649= | |
| ENST00000418664.2:c.6150G>A | ENSP00000396591.2:p.Arg2050= | |
| NM_001008844.1:c.6150G>A | NP_001008844.1:p.Arg2050= | |
| NM_004415.2:c.7947G>A , LRG_423t1:c.7947G>A | NP_004406.2:p.Arg2649= | |
| XM_011514323.1:c.6618G>A | XP_011512625.1:p.Arg2206= | |
| NM_001008844.2:c.6150G>A | NP_001008844.1:p.Arg2050= | |
| NM_001319034.1:c.6618G>A | NP_001305963.1:p.Arg2206= | |
| NM_004415.3:c.7947G>A | NP_004406.2:p.Arg2649= | |
| NM_004415.4:c.7947G>A MANE Select | NP_004406.2:p.Arg2649= | |
| NM_001008844.3:c.6150G>A | NP_001008844.1:p.Arg2050= | |
| NM_001319034.2:c.6618G>A | NP_001305963.1:p.Arg2206= |