Linked Data
ClinVar Variation Id:
284440
dbSNP Id:
rs200463656
ExAC:
22:50512770 G / A
gnomAD v2:
22-50512770-G-A
gnomAD v3:
22-50074341-G-A
gnomAD v4:
22-50074341-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50074341G>A , CM000684.2:g.50074341G>A | GRCh38 |
| NC_000022.10:g.50512770G>A , CM000684.1:g.50512770G>A | GRCh37 |
| NC_000022.9:g.48854897G>A | NCBI36 |
| NG_009162.1:g.16589C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311597.10:c.598-9C>T MANE Select | ENSP00000310375.6:n.598-9C>T | |
| ENST00000311597.9:c.598-9C>T | ENSP00000310375.5:n.598-9C>T | |
| ENST00000395876.6:c.598-9C>T | ENSP00000379216.2:n.598-9C>T | |
| ENST00000442311.1:c.508-9C>T | ENSP00000401385.1:n.508-9C>T | |
| ENST00000470008.1:n.78-9C>T | ||
| NM_015166.3:c.598-9C>T | NP_055981.1:n.598-9C>T | |
| NM_139202.2:c.598-9C>T | NP_631941.1:n.598-9C>T | |
| XM_011530678.1:c.598-9C>T | XP_011528980.1:n.598-9C>T | |
| XR_430476.2:n.993-9C>T | ||
| XM_011530678.2:c.598-9C>T | XP_011528980.1:n.598-9C>T | |
| XM_017028671.1:c.598-9C>T | XP_016884160.1:n.598-9C>T | |
| XR_001755180.2:n.1103-9C>T | ||
| XR_001755181.2:n.871-9C>T | ||
| NM_001376472.1:c.598-9C>T | NP_001363401.1:n.598-9C>T | |
| NM_001376473.1:c.598-9C>T | NP_001363402.1:n.598-9C>T | |
| NM_001376474.1:c.598-9C>T | NP_001363403.1:n.598-9C>T | |
| NM_001376475.1:c.598-9C>T | NP_001363404.1:n.598-9C>T | |
| NM_001376476.1:c.598-9C>T | NP_001363405.1:n.598-9C>T | |
| NM_001376477.1:c.598-9C>T | NP_001363406.1:n.598-9C>T | |
| NM_001376478.1:c.598-9C>T | NP_001363407.1:n.598-9C>T | |
| NM_001376479.1:c.598-9C>T | NP_001363408.1:n.598-9C>T | |
| NM_001376480.1:c.508-9C>T | NP_001363409.1:n.508-9C>T | |
| NM_001376481.1:c.496-9C>T | NP_001363410.1:n.496-9C>T | |
| NM_001376482.1:c.442-9C>T | NP_001363411.1:n.442-9C>T | |
| NM_001376483.1:c.442-9C>T | NP_001363412.1:n.442-9C>T | |
| NM_001376484.1:c.361-9C>T | NP_001363413.1:n.361-9C>T | |
| NM_015166.4:c.598-9C>T MANE Select | NP_055981.1:n.598-9C>T | |
| NM_139202.3:c.598-9C>T | NP_631941.1:n.598-9C>T | |
| NR_164811.1:n.945-9C>T | ||
| NR_164812.1:n.729-9C>T | ||
| NR_164813.1:n.1122-9C>T |