Linked Data
ClinVar Variation Id:
284207
dbSNP Id:
rs148188703
ExAC:
6:24523087 C / T
gnomAD v2:
6-24523087-C-T
gnomAD v3:
6-24522859-C-T
gnomAD v4:
6-24522859-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24522859C>T , CM000668.2:g.24522859C>T | GRCh38 |
| NC_000006.11:g.24523087C>T , CM000668.1:g.24523087C>T | GRCh37 |
| NC_000006.10:g.24631066C>T | NCBI36 |
| NG_008161.1:g.32891C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357578.8:c.1107C>T MANE Select | ENSP00000350191.3:p.Arg369= | |
| ENST00000479394.2:n.222C>T | ||
| ENST00000672352.1:c.726C>T | ENSP00000500876.1:p.Arg242= | |
| ENST00000672619.1:n.467C>T | ||
| ENST00000672652.1:c.1070C>T | ||
| ENST00000348925.2:c.1146C>T | ENSP00000314649.3:p.Arg382= | |
| ENST00000357578.7:c.1107C>T | ENSP00000350191.3:p.Arg369= | |
| ENST00000479394.1:n.222C>T | ||
| ENST00000491546.5:c.1023C>T | ENSP00000417687.1:p.Arg341= | |
| NM_001080.3:c.1107C>T MANE Select | NP_001071.1:p.Arg369= | |
| NM_170740.1:c.1146C>T | NP_733936.1:p.Arg382= | |
| NM_001368954.1:c.963C>T | NP_001355883.1:p.Arg321= |