Linked Data
ClinVar Variation Id:
2950073
ClinVar RCV Id:
RCV003807431
MyVariant Identifiers:
chr11:g.6413213G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6391983G>A , CM000673.2:g.6391983G>A | GRCh38 |
| NC_000011.9:g.6413213G>A , CM000673.1:g.6413213G>A | GRCh37 |
| NC_000011.8:g.6369789G>A | NCBI36 |
| NG_011780.1:g.6559G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000342245.9:c.918G>A MANE Select | ENSP00000340409.4:p.Arg306= | |
| ENST00000342245.8:c.918G>A | ENSP00000340409.4:p.Arg306= | |
| ENST00000526280.1:c.107G>A | ||
| ENST00000527275.5:c.915G>A | ENSP00000435350.1:p.Arg305= | |
| ENST00000530395.1:c.99G>A | ENSP00000431479.1:p.Arg33= | |
| ENST00000531303.5:c.438+480G>A | ENSP00000432625.1:n.438+480G>A | |
| ENST00000533123.5:c.918G>A | ENSP00000435950.1:p.Arg306= | |
| ENST00000533196.1:n.375-23G>A | ||
| ENST00000534405.5:c.918G>A | ENSP00000434353.1:p.Arg306= | |
| NM_000543.4:c.918G>A | NP_000534.3:p.Arg306= | |
| NM_001007593.2:c.915G>A | NP_001007594.2:p.Arg305= | |
| XM_005253075.3:c.918G>A | XP_005253132.1:p.Arg306= | |
| XM_011520303.1:c.918G>A | XP_011518605.1:p.Arg306= | |
| XM_011520304.1:c.918G>A | XP_011518606.1:p.Arg306= | |
| XR_930886.1:n.1216G>A | ||
| NM_001318087.1:c.918G>A | NP_001305016.1:p.Arg306= | |
| NM_001318088.1:c.-44G>A | NP_001305017.1:n.-44G>A | |
| NM_001365135.1:c.918G>A | NP_001352064.1:p.Arg306= | |
| NR_027400.2:n.1103G>A | ||
| NR_134502.1:n.623+480G>A | ||
| XM_011520304.2:c.918G>A | XP_011518606.1:p.Arg306= | |
| XR_001747940.2:n.1043G>A | ||
| XR_002957158.1:n.1043G>A | ||
| NM_000543.5:c.918G>A MANE Select | NP_000534.3:p.Arg306= | |
| NM_001007593.3:c.915G>A | NP_001007594.2:p.Arg305= | |
| NM_001318087.2:c.918G>A | NP_001305016.1:p.Arg306= | |
| NM_001318088.2:c.-44G>A | NP_001305017.1:n.-44G>A | |
| NM_001365135.2:c.918G>A | NP_001352064.1:p.Arg306= | |
| NR_027400.3:n.1043G>A | ||
| NR_134502.2:n.563+480G>A |