Linked Data
ClinVar Variation Id:
1793488
dbSNP Id:
rs746744099
ExAC:
22:19906499 G / A
gnomAD v2:
22-19906499-G-A
gnomAD v3:
22-19918976-G-A
gnomAD v4:
22-19918976-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.19918976G>A , CM000684.2:g.19918976G>A | GRCh38 |
| NC_000022.10:g.19906499G>A , CM000684.1:g.19906499G>A | GRCh37 |
| NC_000022.9:g.18286499G>A | NCBI36 |
| NG_011835.1:g.27861C>T , LRG_417:g.27861C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000400521.7:c.258C>T MANE Select | ENSP00000383365.1:p.Cys86= | |
| ENST00000334363.14:c.258C>T | ENSP00000334451.9:p.Cys86= | |
| ENST00000400518.5:c.168C>T | ENSP00000383362.1:p.Cys56= | |
| ENST00000400519.6:c.255C>T | ENSP00000383363.1:p.Cys85= | |
| ENST00000400521.6:c.258C>T | ENSP00000383365.1:p.Cys86= | |
| ENST00000400525.6:c.189C>T | ENSP00000383369.3:p.Cys63= | |
| ENST00000474308.5:c.201C>T | ENSP00000485665.1:p.Cys67= | |
| ENST00000491939.6:c.162C>T | ENSP00000485543.1:p.Cys54= | |
| ENST00000496729.2:n.263C>T | ||
| ENST00000542719.6:c.-31C>T | ENSP00000485128.2:n.-31C>T | |
| NM_001282512.1:c.258C>T | NP_001269441.1:p.Cys86= | |
| NM_006440.4:c.258C>T | NP_006431.2:p.Cys86= | |
| NM_001282512.2:c.258C>T | NP_001269441.1:p.Cys86= | |
| NM_001352300.1:c.255C>T | NP_001339229.1:p.Cys85= | |
| NM_001352301.1:c.168C>T | NP_001339230.1:p.Cys56= | |
| NM_001352302.1:c.-31C>T | NP_001339231.1:n.-31C>T | |
| NM_001352303.1:c.162C>T | NP_001339232.1:p.Cys54= | |
| NR_147957.1:n.390C>T | ||
| NM_006440.5:c.258C>T MANE Select | NP_006431.2:p.Cys86= | |
| NM_001282512.3:c.258C>T | NP_001269441.1:p.Cys86= | |
| NM_001352300.2:c.255C>T | NP_001339229.1:p.Cys85= | |
| NR_147957.2:n.216C>T | ||
| NM_001352301.2:c.168C>T | NP_001339230.1:p.Cys56= | |
| NM_001352302.2:c.-31C>T | NP_001339231.1:n.-31C>T | |
| NM_001352303.2:c.162C>T | NP_001339232.1:p.Cys54= |