Linked Data
ClinVar Variation Id:
2815371
ClinVar RCV Id:
RCV003755464
MyVariant Identifiers:
chr4:g.997171C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.1003383C>G , CM000666.2:g.1003383C>G | GRCh38 |
| NC_000004.11:g.997171C>G , CM000666.1:g.997171C>G | GRCh37 |
| NC_000004.10:g.987171C>G | NCBI36 |
| NG_008103.1:g.21387C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000247933.9:c.1563C>G | ENSP00000247933.4:p.Gly521= | |
| ENST00000514224.2:c.1563C>G MANE Select | ENSP00000425081.2:p.Gly521= | |
| ENST00000652070.1:n.1619C>G | ||
| ENST00000247933.8:c.1563C>G | ENSP00000247933.4:p.Gly521= | |
| ENST00000502829.1:n.552C>G | ||
| ENST00000514224.1:c.1167C>G | ENSP00000425081.1:p.Gly389= | |
| ENST00000514698.5:n.1670C>G | ||
| NM_000203.4:c.1563C>G | NP_000194.2:p.Gly521= | |
| NR_110313.1:n.1651C>G | ||
| XM_006713882.2:c.1167C>G | XP_006713945.1:p.Gly389= | |
| XM_011513459.1:c.1629C>G | XP_011511761.1:p.Gly543= | |
| XM_011513460.1:c.1422C>G | XP_011511762.1:p.Gly474= | |
| XM_011513461.1:c.1356C>G | XP_011511763.1:p.Gly452= | |
| XM_011513462.1:c.1275C>G | XP_011511764.1:p.Gly425= | |
| XM_011513463.1:c.1275C>G | XP_011511765.1:p.Gly425= | |
| XR_924947.1:n.1819C>G | ||
| NM_000203.5:c.1563C>G MANE Select | NP_000194.2:p.Gly521= | |
| NM_001363576.1:c.1167C>G | NP_001350505.1:p.Gly389= | |
| XM_011513461.2:c.1356C>G | XP_011511763.1:p.Gly452= | |
| XM_017008163.1:c.603C>G | XP_016863652.1:p.Gly201= |