Linked Data
ClinVar Variation Id:
1992256
ClinVar RCV Id:
RCV002814332
MyVariant Identifiers:
chr6:g.129802557T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.129481412T>C , CM000668.2:g.129481412T>C | GRCh38 |
| NC_000006.11:g.129802557T>C , CM000668.1:g.129802557T>C | GRCh37 |
| NC_000006.10:g.129844250T>C | NCBI36 |
| NG_008678.1:g.603272T>C , LRG_409:g.603272T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000617695.5:c.7710T>C | ENSP00000481744.2:p.Pro2570= | |
| ENST00000618192.5:c.7986T>C | ENSP00000480802.2:p.Pro2662= | |
| ENST00000421865.3:c.7722T>C MANE Select | ENSP00000400365.2:p.Pro2574= | |
| ENST00000421865.2:c.7722T>C | ENSP00000400365.2:p.Pro2574= | |
| ENST00000617695.4:c.7710T>C | ENSP00000481744.1:p.Pro2570= | |
| ENST00000618192.4:c.7719T>C | ENSP00000480802.1:p.Pro2573= | |
| NM_000426.3:c.7722T>C , LRG_409t1:c.7722T>C | NP_000417.2:p.Pro2574= | |
| NM_001079823.1:c.7710T>C | NP_001073291.1:p.Pro2570= | |
| XM_005266981.2:c.7986T>C | XP_005267038.1:p.Pro2662= | |
| XM_005266982.2:c.7974T>C | XP_005267039.1:p.Pro2658= | |
| XM_011535820.1:c.7980T>C | XP_011534122.1:p.Pro2660= | |
| XM_005266981.3:c.7986T>C | XP_005267038.1:p.Pro2662= | |
| XM_005266982.3:c.7974T>C | XP_005267039.1:p.Pro2658= | |
| XM_011535820.2:c.7980T>C | XP_011534122.1:p.Pro2660= | |
| XM_017010851.2:c.7992T>C | XP_016866340.1:p.Pro2664= | |
| XM_017010852.1:c.6117T>C | XP_016866341.1:p.Pro2039= | |
| NM_000426.4:c.7722T>C MANE Select | NP_000417.3:p.Pro2574= | |
| NM_001079823.2:c.7710T>C | NP_001073291.2:p.Pro2570= |