Linked Data
ClinVar Variation Id:
432635
dbSNP Id:
rs113755498
ExAC:
2:238277212 G / A
gnomAD v2:
2-238277212-G-A
gnomAD v3:
2-237368569-G-A
gnomAD v4:
2-237368569-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.237368569G>A , CM000664.2:g.237368569G>A | GRCh38 |
| NC_000002.11:g.238277212G>A , CM000664.1:g.238277212G>A | GRCh37 |
| NC_000002.10:g.237941951G>A | NCBI36 |
| NG_008676.1:g.50639C>T , LRG_473:g.50639C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000353578.9:c.4276C>T | ENSP00000315873.4:p.Arg1426Trp | |
| ENST00000684597.1:c.224C>T | ||
| ENST00000295550.9:c.4894C>T MANE Select | ENSP00000295550.4:p.Arg1632Trp | |
| ENST00000295550.8:c.4894C>T | ENSP00000295550.4:p.Arg1632Trp | |
| ENST00000347401.7:c.3073C>T | ENSP00000315609.4:p.Arg1025Trp | |
| ENST00000353578.8:c.4276C>T | ENSP00000315873.4:p.Arg1426Trp | |
| ENST00000409809.5:c.4276C>T | ENSP00000386844.1:p.Arg1426Trp | |
| ENST00000472056.5:c.3073C>T | ENSP00000418285.1:p.Arg1025Trp | |
| NM_004369.3:c.4894C>T , LRG_473t1:c.4894C>T | NP_004360.2:p.Arg1632Trp | |
| NM_057166.4:c.3073C>T | NP_476507.3:p.Arg1025Trp | |
| NM_057167.3:c.4276C>T | NP_476508.2:p.Arg1426Trp | |
| XM_005246065.1:c.4294C>T | XP_005246122.1:p.Arg1432Trp | |
| XM_005246066.1:c.3673C>T | XP_005246123.1:p.Arg1225Trp | |
| XM_006712253.1:c.4393C>T | XP_006712316.1:p.Arg1465Trp | |
| XM_011510574.1:c.4891C>T | XP_011508876.1:p.Arg1631Trp | |
| XM_011510575.1:c.2488C>T | XP_011508877.1:p.Arg830Trp | |
| XM_017003304.1:c.2488C>T | XP_016858793.1:p.Arg830Trp | |
| XM_024452684.1:c.3673C>T | XP_024308452.1:p.Arg1225Trp | |
| NM_004369.4:c.4894C>T MANE Select | NP_004360.2:p.Arg1632Trp | |
| NM_057166.5:c.3073C>T | NP_476507.3:p.Arg1025Trp | |
| NM_057167.4:c.4276C>T | NP_476508.2:p.Arg1426Trp |