Linked Data
ClinVar Variation Id:
2950492
ClinVar RCV Id:
RCV003809802
MyVariant Identifiers:
chr21:g.34003728T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.32631418T>C , CM000683.2:g.32631418T>C | GRCh38 |
| NC_000021.8:g.34003728T>C , CM000683.1:g.34003728T>C | GRCh37 |
| NC_000021.7:g.32925599T>C | NCBI36 |
| NG_030017.1:g.101624A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382499.7:c.4440A>G | ENSP00000371939.2:n.4440A>G | |
| ENST00000433931.7:c.4416A>G | ENSP00000409667.2:p.Glu1472= | |
| ENST00000630077.3:c.4158A>G | ENSP00000487560.1:p.Glu1386= | |
| ENST00000674204.1:c.*387A>G | ENSP00000501504.1:n.*387A>G | |
| ENST00000674308.1:c.4299A>G | ENSP00000501426.1:p.Glu1433= | |
| ENST00000674351.1:c.*387A>G MANE Select | ENSP00000501530.1:n.*387A>G | |
| ENST00000357345.7:c.*387A>G | ENSP00000349903.3:n.*387A>G | |
| ENST00000382491.7:c.*387A>G | ENSP00000371931.4:n.*387A>G | |
| ENST00000382499.6:c.4440A>G | ENSP00000371939.2:n.4440A>G | |
| ENST00000433931.6:c.4416A>G | ENSP00000409667.2:p.Glu1472= | |
| ENST00000438952.5:c.949A>G | ||
| ENST00000630077.2:c.4158A>G | ENSP00000487560.1:p.Glu1386= | |
| NM_001160302.1:c.*387A>G | NP_001153774.1:n.*387A>G | |
| NM_001160306.1:c.4158A>G | NP_001153778.1:p.Glu1386= | |
| NM_003895.3:c.4416A>G | NP_003886.3:p.Glu1472= | |
| NM_203446.2:c.4440A>G | NP_982271.2:n.4440A>G | |
| XM_017028494.1:c.4251A>G | XP_016883983.1:p.Glu1417= | |
| XM_017028495.2:c.4401A>G | XP_016883984.1:p.Glu1467= | |
| XM_017028496.1:c.4212A>G | XP_016883985.1:p.Glu1404= | |
| XM_017028497.2:c.4368A>G | XP_016883986.1:p.Glu1456= | |
| XM_017028498.1:c.4173A>G | XP_016883987.1:p.Glu1391= | |
| XM_017028499.2:c.4275A>G | XP_016883988.1:p.Glu1425= | |
| XM_017028500.1:c.*387A>G | XP_016883989.1:n.*387A>G | |
| XM_017028501.1:c.*387A>G | XP_016883990.1:n.*387A>G | |
| XM_017028502.1:c.*387A>G | XP_016883991.1:n.*387A>G | |
| XM_017028503.1:c.*387A>G | XP_016883992.1:n.*387A>G | |
| XM_017028504.1:c.*387A>G | XP_016883993.1:n.*387A>G | |
| XM_017028505.2:c.*387A>G | XP_016883994.1:n.*387A>G | |
| NM_001160306.2:c.4158A>G | NP_001153778.1:p.Glu1386= | |
| NM_203446.3:c.*387A>G MANE Select | NP_982271.3:n.*387A>G |