Linked Data
ClinVar Variation Id:
1763272
dbSNP Id:
rs1893007191
gnomAD v4:
15-66485136-A-G
MyVariant Identifiers:
chr15:g.66777474A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.66485136A>G , CM000677.2:g.66485136A>G | GRCh38 |
| NC_000015.9:g.66777474A>G , CM000677.1:g.66777474A>G | GRCh37 |
| NC_000015.8:g.64564528A>G | NCBI36 |
| NG_008305.1:g.103264A>G , LRG_725:g.103264A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684779.1:c.628-2092A>G | ENSP00000508681.1:n.628-2092A>G | |
| ENST00000685172.1:c.840A>G | ENSP00000509604.1:p.Glu280= | |
| ENST00000685763.1:c.693A>G | ENSP00000509016.1:p.Glu231= | |
| ENST00000686347.1:c.569-2092A>G | ENSP00000509027.1:n.569-2092A>G | |
| ENST00000687191.1:n.1198A>G | ||
| ENST00000687481.1:n.255A>G | ||
| ENST00000689951.1:c.891A>G | ENSP00000509308.1:p.Glu297= | |
| ENST00000691077.1:c.*77A>G | ENSP00000509843.1:n.*77A>G | |
| ENST00000691576.1:c.711A>G | ENSP00000510066.1:p.Glu237= | |
| ENST00000691937.1:c.840A>G | ENSP00000508768.1:p.Glu280= | |
| ENST00000692487.1:c.*77A>G | ENSP00000509534.1:n.*77A>G | |
| ENST00000692683.1:c.774A>G | ENSP00000508437.1:p.Glu258= | |
| ENST00000693150.1:c.696A>G | ENSP00000510309.1:p.Glu232= | |
| ENST00000307102.10:c.840A>G MANE Select | ENSP00000302486.5:p.Glu280= | |
| ENST00000307102.9:c.840A>G | ENSP00000302486.4:p.Glu280= | |
| ENST00000566326.1:c.312A>G | ENSP00000456438.1:p.Glu104= | |
| NM_002755.3:c.840A>G , LRG_725t1:c.840A>G | NP_002746.1:p.Glu280= | |
| XM_011521783.1:c.774A>G | XP_011520085.1:p.Glu258= | |
| XM_011521783.3:c.774A>G | XP_011520085.1:p.Glu258= | |
| XM_017022411.2:c.762A>G | XP_016877900.1:p.Glu254= | |
| XM_017022412.1:c.696A>G | XP_016877901.1:p.Glu232= | |
| XM_017022413.1:c.312A>G | XP_016877902.1:p.Glu104= | |
| NM_002755.4:c.840A>G MANE Select | NP_002746.1:p.Glu280= |