Linked Data
ClinVar Variation Id:
927898
ClinVar RCV Id:
RCV001191470
dbSNP Id:
rs1759495786
gnomAD v4:
6-7583025-C-T
MyVariant Identifiers:
chr6:g.7583258C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.7583025C>T , CM000668.2:g.7583025C>T | GRCh38 |
| NC_000006.11:g.7583258C>T , CM000668.1:g.7583258C>T | GRCh37 |
| NC_000006.10:g.7528257C>T | NCBI36 |
| NG_008803.1:g.46389C>T , LRG_423:g.46389C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710359.1:c.4434C>T | ENSP00000518230.1:p.Thr1478= | |
| ENST00000379802.8:c.5763C>T MANE Select | ENSP00000369129.3:p.Thr1921= | |
| ENST00000379802.7:c.5763C>T | ENSP00000369129.3:p.Thr1921= | |
| ENST00000418664.2:c.3966C>T | ENSP00000396591.2:p.Thr1322= | |
| NM_001008844.1:c.3966C>T | NP_001008844.1:p.Thr1322= | |
| NM_004415.2:c.5763C>T , LRG_423t1:c.5763C>T | NP_004406.2:p.Thr1921= | |
| XM_011514323.1:c.4434C>T | XP_011512625.1:p.Thr1478= | |
| NM_001008844.2:c.3966C>T | NP_001008844.1:p.Thr1322= | |
| NM_001319034.1:c.4434C>T | NP_001305963.1:p.Thr1478= | |
| NM_004415.3:c.5763C>T | NP_004406.2:p.Thr1921= | |
| NM_004415.4:c.5763C>T MANE Select | NP_004406.2:p.Thr1921= | |
| NM_001008844.3:c.3966C>T | NP_001008844.1:p.Thr1322= | |
| NM_001319034.2:c.4434C>T | NP_001305963.1:p.Thr1478= |