Linked Data
ClinVar Variation Id:
132683
dbSNP Id:
rs17857111
gnomAD v4:
21-34449540-C-T
COSMIC:
COSM4409001
MyVariant Identifiers:
chr21:g.34449540C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.34449540C>T , CM000683.2:g.34449540C>T | GRCh38 |
| NG_009091.1:g.66776G>A , LRG_290:g.66776G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000399286.3:c.95G>A MANE Select | ENSP00000382226.2:p.Arg32His | |
| ENST00000337385.7:c.95G>A | ENSP00000337255.3:p.Arg32His | |
| ENST00000399284.1:c.95G>A | ENSP00000382225.1:p.Arg32His | |
| ENST00000399286.2:c.95G>A | ENSP00000382226.2:p.Arg32His | |
| ENST00000399289.7:c.95G>A | ENSP00000382228.3:p.Arg32His | |
| ENST00000416357.6:c.95G>A | ENSP00000416258.2:p.Arg32His | |
| ENST00000432085.5:c.95G>A | ENSP00000412498.1:p.Arg32His | |
| ENST00000611936.1:c.95G>A | ENSP00000478215.1:p.Arg32His | |
| ENST00000621601.4:c.95G>A | ENSP00000483895.1:p.Arg32His | |
| NM_000219.5:c.95G>A | NP_000210.2:p.Arg32His | |
| NM_001127668.3:c.95G>A | NP_001121140.1:p.Arg32His | |
| NM_001127669.3:c.95G>A | NP_001121141.1:p.Arg32His | |
| NM_001127670.3:c.95G>A | NP_001121142.1:p.Arg32His | |
| NM_001270402.2:c.95G>A | NP_001257331.1:p.Arg32His | |
| NM_001270403.2:c.95G>A | NP_001257332.1:p.Arg32His | |
| NM_001270404.2:c.95G>A | NP_001257333.1:p.Arg32His | |
| NM_001270405.2:c.95G>A | NP_001257334.1:p.Arg32His | |
| XM_011529555.1:c.13+5846G>A | XP_011527857.1:n.13+5846G>A | |
| XM_011529557.1:c.279+9114G>A | XP_011527859.1:n.279+9114G>A | |
| XM_017028342.1:c.158G>A | XP_016883831.1:p.Arg53His | |
| NM_000219.6:c.95G>A MANE Select | NP_000210.2:p.Arg32His | |
| NM_001127669.4:c.95G>A | NP_001121141.1:p.Arg32His | |
| NM_001127668.4:c.95G>A | NP_001121140.1:p.Arg32His | |
| NM_001127670.4:c.95G>A | NP_001121142.1:p.Arg32His | |
| NM_001270402.3:c.95G>A | NP_001257331.1:p.Arg32His | |
| NM_001270404.3:c.95G>A | NP_001257333.1:p.Arg32His | |
| NM_001270405.3:c.95G>A | NP_001257334.1:p.Arg32His |