Linked Data
ClinVar Variation Id:
3025219
ClinVar RCV Id:
RCV003886095
dbSNP Id:
rs1380402120
gnomAD v2:
22-50962434-A-G
gnomAD v4:
22-50524005-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50524005A>G , CM000684.2:g.50524005A>G | GRCh38 |
| NC_000022.10:g.50962434A>G , CM000684.1:g.50962434A>G | GRCh37 |
| NC_000022.9:g.49309300A>G | NCBI36 |
| NG_011860.1:g.11081T>C , LRG_727:g.11081T>C | |
| NG_016235.1:g.7435T>C | |
| NG_021419.1:g.20790A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395693.8:c.407T>C (SCO2) MANE Select | ENSP00000379046.4:p.Ile136Thr | |
| ENST00000420993.7:c.*630A>G (NCAPH2) MANE Select | ENSP00000410088.2:n.*630A>G | |
| ENST00000543927.6:c.407T>C (SCO2) | ENSP00000444433.1:p.Ile136Thr | |
| ENST00000638598.2:c.407T>C (SCO2) | ENSP00000491753.2:p.Ile136Thr | |
| ENST00000252785.3:c.407T>C | ENSP00000252785.3:p.Ile136Thr | |
| ENST00000395693.7:c.407T>C | ENSP00000379046.3:p.Ile136Thr | |
| ENST00000423348.1:c.407T>C | ENSP00000403570.1:p.Ile136Thr | |
| ENST00000439934.5:c.407T>C | ENSP00000415642.1:p.Ile136Thr | |
| ENST00000535425.5:c.407T>C | ENSP00000444242.1:p.Ile136Thr | |
| ENST00000543927.5:c.407T>C | ENSP00000444433.1:p.Ile136Thr | |
| NM_001169109.1:c.407T>C (SCO2) | NP_001162580.1:p.Ile136Thr | |
| NM_001169110.1:c.407T>C (SCO2) | NP_001162581.1:p.Ile136Thr | |
| NM_001169111.1:c.407T>C (SCO2) | NP_001162582.1:p.Ile136Thr | |
| NM_001185011.1:c.*630A>G (NCAPH2) | NP_001171940.1:n.*630A>G | |
| NM_005138.2:c.407T>C (SCO2) | NP_005129.2:p.Ile136Thr | |
| NM_152299.3:c.*630A>G (NCAPH2) | NP_689512.2:n.*630A>G | |
| XR_001755232.1:n.2658A>G (NCAPH2) | ||
| NM_152299.4:c.*630A>G (NCAPH2) MANE Select | NP_689512.2:n.*630A>G | |
| NM_001185011.2:c.*630A>G (NCAPH2) | NP_001171940.1:n.*630A>G | |
| NM_005138.3:c.407T>C (SCO2) MANE Select | NP_005129.2:p.Ile136Thr | |
| NM_001169109.2:c.407T>C (SCO2) | NP_001162580.1:p.Ile136Thr | |
| NM_001169111.2:c.407T>C (SCO2) | NP_001162582.1:p.Ile136Thr |