Linked Data
dbSNP Id:
rs770306064
ExAC:
22:50662876 T / C
gnomAD v2:
22-50662876-T-C
gnomAD v4:
22-50224447-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50224447T>C , CM000684.2:g.50224447T>C | GRCh38 |
| NC_000022.10:g.50662876T>C , CM000684.1:g.50662876T>C | GRCh37 |
| NC_000022.9:g.49005003T>C | NCBI36 |
| NG_032160.1:g.25525A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248846.10:c.2066-27A>G MANE Select | ENSP00000248846.5:n.2066-27A>G | |
| ENST00000248846.9:c.2066-27A>G | ENSP00000248846.5:n.2066-27A>G | |
| ENST00000439308.6:c.2066-27A>G | ENSP00000397387.2:n.2066-27A>G | |
| ENST00000473946.1:n.375-27A>G | ||
| ENST00000489511.5:n.83-27A>G | ||
| ENST00000491449.5:n.373-27A>G | ||
| ENST00000498611.5:n.2599-27A>G | ||
| NM_020461.3:c.2066-27A>G | NP_065194.2:n.2066-27A>G | |
| XR_938347.1:n.2631-27A>G | ||
| XR_938348.1:n.2631-27A>G | ||
| XR_001755343.2:n.2635-27A>G | ||
| XR_001755344.2:n.2635-27A>G | ||
| XR_002958720.1:n.2635-27A>G | ||
| XR_938347.2:n.2635-27A>G | ||
| NM_020461.4:c.2066-27A>G MANE Select | NP_065194.3:n.2066-27A>G |