Linked Data
ClinVar Variation Id:
902939
dbSNP Id:
rs147624681
ExAC:
22:50962300 C / T
gnomAD v2:
22-50962300-C-T
gnomAD v3:
22-50523871-C-T
gnomAD v4:
22-50523871-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50523871C>T , CM000684.2:g.50523871C>T | GRCh38 |
| NC_000022.10:g.50962300C>T , CM000684.1:g.50962300C>T | GRCh37 |
| NC_000022.9:g.49309166C>T | NCBI36 |
| NG_011860.1:g.11215G>A , LRG_727:g.11215G>A | |
| NG_016235.1:g.7569G>A | |
| NG_021419.1:g.20656C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395693.8:c.541G>A (SCO2) MANE Select | ENSP00000379046.4:p.Val181Ile | |
| ENST00000420993.7:c.*496C>T (NCAPH2) MANE Select | ENSP00000410088.2:n.*496C>T | |
| ENST00000543927.6:c.541G>A (SCO2) | ENSP00000444433.1:p.Val181Ile | |
| ENST00000252785.3:c.541G>A | ENSP00000252785.3:p.Val181Ile | |
| ENST00000395693.7:c.541G>A | ENSP00000379046.3:p.Val181Ile | |
| ENST00000535425.5:c.541G>A | ENSP00000444242.1:p.Val181Ile | |
| ENST00000543927.5:c.541G>A | ENSP00000444433.1:p.Val181Ile | |
| NM_001169109.1:c.541G>A (SCO2) | NP_001162580.1:p.Val181Ile | |
| NM_001169110.1:c.541G>A (SCO2) | NP_001162581.1:p.Val181Ile | |
| NM_001169111.1:c.541G>A (SCO2) | NP_001162582.1:p.Val181Ile | |
| NM_001185011.1:c.*496C>T (NCAPH2) | NP_001171940.1:n.*496C>T | |
| NM_005138.2:c.541G>A (SCO2) | NP_005129.2:p.Val181Ile | |
| NM_152299.3:c.*496C>T (NCAPH2) | NP_689512.2:n.*496C>T | |
| XR_001755232.1:n.2524C>T (NCAPH2) | ||
| NM_152299.4:c.*496C>T (NCAPH2) MANE Select | NP_689512.2:n.*496C>T | |
| NM_001185011.2:c.*496C>T (NCAPH2) | NP_001171940.1:n.*496C>T | |
| NM_005138.3:c.541G>A (SCO2) MANE Select | NP_005129.2:p.Val181Ile | |
| NM_001169109.2:c.541G>A (SCO2) | NP_001162580.1:p.Val181Ile | |
| NM_001169111.2:c.541G>A (SCO2) | NP_001162582.1:p.Val181Ile |