Linked Data
dbSNP Id:
rs777904210
ExAC:
22:50659175 T / C
gnomAD v2:
22-50659175-T-C
gnomAD v3:
22-50220746-T-C
gnomAD v4:
22-50220746-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50220746T>C , CM000684.2:g.50220746T>C | GRCh38 |
| NC_000022.10:g.50659175T>C , CM000684.1:g.50659175T>C | GRCh37 |
| NC_000022.9:g.49001302T>C | NCBI36 |
| NG_032160.1:g.29226A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248846.10:c.3613A>G MANE Select | ENSP00000248846.5:p.Met1205Val | |
| ENST00000248846.9:c.3613A>G | ENSP00000248846.5:p.Met1205Val | |
| ENST00000439308.6:c.3613A>G | ENSP00000397387.2:p.Met1205Val | |
| ENST00000491449.5:n.1920A>G | ||
| ENST00000498611.5:n.3617+529A>G | ||
| NM_020461.3:c.3613A>G | NP_065194.2:p.Met1205Val | |
| XR_938347.1:n.4178A>G | ||
| XR_938348.1:n.3050-731A>G | ||
| XR_001755343.2:n.4182A>G | ||
| XR_001755344.2:n.4182A>G | ||
| XR_002958720.1:n.3054-731A>G | ||
| XR_938347.2:n.4182A>G | ||
| NM_020461.4:c.3613A>G MANE Select | NP_065194.3:p.Met1205Val |