Linked Data
ClinVar Variation Id:
341127
ClinVar RCV Id:
RCV000348941
dbSNP Id:
rs886057367
gnomAD v3:
22-29696805-T-G
gnomAD v4:
22-29696805-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.29696805T>G , CM000684.2:g.29696805T>G | GRCh38 |
| NC_000022.10:g.30092794T>G , CM000684.1:g.30092794T>G | GRCh37 |
| NC_000022.9:g.28422794T>G | NCBI36 |
| NG_009057.1:g.98250T>G , LRG_511:g.98250T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000338641.10:c.*2003T>G MANE Select | ENSP00000344666.5:n.*2003T>G | |
| ENST00000672461.1:c.*502-456T>G | ENSP00000500919.1:n.*502-456T>G | |
| ENST00000672896.1:c.*2063T>G | ENSP00000500117.1:n.*2063T>G | |
| ENST00000338641.8:c.*2003T>G | ENSP00000344666.4:n.*2003T>G | |
| ENST00000361452.8:c.*2063T>G | ENSP00000354897.4:n.*2063T>G | |
| ENST00000413209.6:c.*2003T>G | ENSP00000409921.2:n.*2003T>G | |
| NM_000268.3:c.*2003T>G , LRG_511t1:c.*2003T>G | NP_000259.1:n.*2003T>G | |
| NM_016418.5:c.*2063T>G , LRG_511t2:c.*2063T>G | NP_057502.2:n.*2063T>G | |
| NM_181828.2:c.*2063T>G | NP_861966.1:n.*2063T>G | |
| NM_181829.2:c.*2063T>G | NP_861967.1:n.*2063T>G | |
| NM_181830.2:c.*2063T>G | NP_861968.1:n.*2063T>G | |
| NM_181832.2:c.*2078T>G | NP_861970.1:n.*2078T>G | |
| NM_181833.2:c.*2003T>G | NP_861971.1:n.*2003T>G | |
| NR_156186.1:n.4350T>G | ||
| XM_017028810.1:c.*2063T>G | XP_016884299.1:n.*2063T>G | |
| NM_000268.4:c.*2003T>G MANE Select | NP_000259.1:n.*2003T>G | |
| NM_181828.3:c.*2063T>G | NP_861966.1:n.*2063T>G | |
| NM_181829.3:c.*2063T>G | NP_861967.1:n.*2063T>G | |
| NM_181830.3:c.*2063T>G | NP_861968.1:n.*2063T>G | |
| NM_181832.3:c.*2078T>G | NP_861970.1:n.*2078T>G | |
| NR_156186.2:n.4273T>G | ||
| NM_181833.3:c.*2003T>G | NP_861971.1:n.*2003T>G |