Linked Data
ClinVar Variation Id:
2810900
ClinVar RCV Id:
RCV003610132
MyVariant Identifiers:
chr2:g.73717084A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.73489957A>G , CM000664.2:g.73489957A>G | GRCh38 |
| NC_000002.11:g.73717084A>G , CM000664.1:g.73717084A>G | GRCh37 |
| NC_000002.10:g.73570592A>G | NCBI36 |
| NG_011690.1:g.109205A>G , LRG_741:g.109205A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682565.1:c.7617A>G | ENSP00000507671.1:p.Lys2539= | |
| ENST00000682801.1:c.7617A>G | ENSP00000507862.1:p.Lys2539= | |
| ENST00000682859.1:c.7617A>G | ENSP00000508222.1:p.Lys2539= | |
| ENST00000683791.1:c.1009A>G | ||
| ENST00000684460.1:c.5069A>G | ||
| ENST00000684548.1:c.7617A>G | ENSP00000507421.1:p.Lys2539= | |
| ENST00000684590.1:c.2064A>G | ENSP00000507376.1:p.Lys688= | |
| ENST00000684656.1:c.5069A>G | ||
| ENST00000613296.6:c.7998A>G MANE Select | ENSP00000482968.1:p.Lys2666= | |
| ENST00000651434.1:c.896-29818A>G | ||
| ENST00000423048.5:c.2829A>G | ENSP00000399833.1:p.Lys943= | |
| ENST00000484298.5:c.7872A>G | ENSP00000478155.1:p.Lys2624= | |
| ENST00000613296.4:c.7998A>G | ENSP00000482968.1:p.Lys2666= | |
| ENST00000614410.4:c.7998A>G | ENSP00000479094.1:p.Lys2666= | |
| ENST00000620466.4:n.1801A>G | ||
| NM_015120.4:c.8001A>G , LRG_741t1:c.8001A>G | NP_055935.4:p.Lys2667= | |
| NM_001378454.1:c.7998A>G MANE Select | NP_001365383.1:p.Lys2666= |