Linked Data
ClinVar Variation Id:
2924311
ClinVar RCV Id:
RCV003786061
dbSNP Id:
rs762381028
ExAC:
6:7585331 C / G
gnomAD v2:
6-7585331-C-G
gnomAD v4:
6-7585098-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.7585098C>G , CM000668.2:g.7585098C>G | GRCh38 |
| NC_000006.11:g.7585331C>G , CM000668.1:g.7585331C>G | GRCh37 |
| NC_000006.10:g.7530330C>G | NCBI36 |
| NG_008803.1:g.48462C>G , LRG_423:g.48462C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710359.1:c.6507C>G | ENSP00000518230.1:p.Thr2169= | |
| ENST00000379802.8:c.7836C>G MANE Select | ENSP00000369129.3:p.Thr2612= | |
| ENST00000379802.7:c.7836C>G | ENSP00000369129.3:p.Thr2612= | |
| ENST00000418664.2:c.6039C>G | ENSP00000396591.2:p.Thr2013= | |
| NM_001008844.1:c.6039C>G | NP_001008844.1:p.Thr2013= | |
| NM_004415.2:c.7836C>G , LRG_423t1:c.7836C>G | NP_004406.2:p.Thr2612= | |
| XM_011514323.1:c.6507C>G | XP_011512625.1:p.Thr2169= | |
| NM_001008844.2:c.6039C>G | NP_001008844.1:p.Thr2013= | |
| NM_001319034.1:c.6507C>G | NP_001305963.1:p.Thr2169= | |
| NM_004415.3:c.7836C>G | NP_004406.2:p.Thr2612= | |
| NM_004415.4:c.7836C>G MANE Select | NP_004406.2:p.Thr2612= | |
| NM_001008844.3:c.6039C>G | NP_001008844.1:p.Thr2013= | |
| NM_001319034.2:c.6507C>G | NP_001305963.1:p.Thr2169= |