Linked Data
ClinVar Variation Id:
1104717
ClinVar RCV Id:
RCV001428859
dbSNP Id:
rs2146872655
MyVariant Identifiers:
chr22:g.30035180A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.29639191A>G , CM000684.2:g.29639191A>G | GRCh38 |
| NC_000022.10:g.30035180A>G , CM000684.1:g.30035180A>G | GRCh37 |
| NC_000022.9:g.28365180A>G | NCBI36 |
| NG_009057.1:g.40636A>G , LRG_511:g.40636A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361166.10:c.342A>G | ENSP00000354529.6:p.Thr114= | |
| ENST00000673312.2:c.342A>G | ENSP00000500186.2:p.Thr114= | |
| ENST00000338641.10:c.342A>G MANE Select | ENSP00000344666.5:p.Thr114= | |
| ENST00000672461.1:c.342A>G | ENSP00000500919.1:p.Thr114= | |
| ENST00000672805.1:c.*224A>G | ENSP00000500295.1:n.*224A>G | |
| ENST00000672896.1:c.342A>G | ENSP00000500117.1:p.Thr114= | |
| ENST00000673312.1:c.255A>G | ENSP00000500186.1:p.Thr85= | |
| ENST00000334961.11:c.115-3011A>G | ENSP00000335652.7:n.115-3011A>G | |
| ENST00000338641.8:c.342A>G | ENSP00000344666.4:p.Thr114= | |
| ENST00000353887.8:c.115-3011A>G | ENSP00000340626.4:n.115-3011A>G | |
| ENST00000361166.8:c.342A>G | ENSP00000354529.4:p.Thr114= | |
| ENST00000361452.8:c.240+2315A>G | ENSP00000354897.4:n.240+2315A>G | |
| ENST00000361676.8:c.216A>G | ENSP00000355183.4:p.Thr72= | |
| ENST00000397789.3:c.342A>G | ENSP00000380891.3:p.Thr114= | |
| ENST00000403435.5:c.342A>G | ENSP00000384029.1:p.Thr114= | |
| ENST00000403999.7:c.342A>G | ENSP00000384797.3:p.Thr114= | |
| ENST00000413209.6:c.342A>G | ENSP00000409921.2:p.Thr114= | |
| ENST00000432151.5:c.115-3011A>G | ENSP00000395885.1:n.115-3011A>G | |
| NM_000268.3:c.342A>G , LRG_511t1:c.342A>G | NP_000259.1:p.Thr114= | |
| NM_016418.5:c.342A>G , LRG_511t2:c.342A>G | NP_057502.2:p.Thr114= | |
| NM_181825.2:c.342A>G | NP_861546.1:p.Thr114= | |
| NM_181828.2:c.216A>G | NP_861966.1:p.Thr72= | |
| NM_181829.2:c.240+2315A>G | NP_861967.1:n.240+2315A>G | |
| NM_181830.2:c.115-3011A>G | NP_861968.1:n.115-3011A>G | |
| NM_181831.2:c.115-3011A>G | NP_861969.1:n.115-3011A>G | |
| NM_181832.2:c.342A>G | NP_861970.1:p.Thr114= | |
| NM_181833.2:c.342A>G | NP_861971.1:p.Thr114= | |
| NR_156186.1:n.901A>G | ||
| XM_017028809.2:c.228A>G | XP_016884298.1:p.Thr76= | |
| XM_017028810.1:c.228A>G | XP_016884299.1:p.Thr76= | |
| NM_000268.4:c.342A>G MANE Select | NP_000259.1:p.Thr114= | |
| NM_181825.3:c.342A>G | NP_861546.1:p.Thr114= | |
| NM_181828.3:c.216A>G | NP_861966.1:p.Thr72= | |
| NM_181829.3:c.240+2315A>G | NP_861967.1:n.240+2315A>G | |
| NM_181830.3:c.115-3011A>G | NP_861968.1:n.115-3011A>G | |
| NM_181831.3:c.115-3011A>G | NP_861969.1:n.115-3011A>G | |
| NM_181832.3:c.342A>G | NP_861970.1:p.Thr114= | |
| NR_156186.2:n.824A>G | ||
| NM_181833.3:c.342A>G | NP_861971.1:p.Thr114= |