Linked Data
ClinVar Variation Id:
3015272
ClinVar RCV Id:
RCV003870879
dbSNP Id:
rs537544870
ExAC:
10:73121834 C / T
gnomAD v2:
10-73121834-C-T
gnomAD v3:
10-71362077-C-T
gnomAD v4:
10-71362077-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.71362077C>T , CM000672.2:g.71362077C>T | GRCh38 |
| NC_000010.10:g.73121834C>T , CM000672.1:g.73121834C>T | GRCh37 |
| NC_000010.9:g.72791840C>T | NCBI36 |
| NG_017066.1:g.47825C>T | |
| NG_017066.2:g.47819C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000697843.1:n.2373C>T | ||
| ENST00000373189.6:c.897C>T MANE Select | ENSP00000362285.5:p.Arg299= | |
| ENST00000479577.2:c.663C>T | ENSP00000493995.1:p.Arg221= | |
| ENST00000642198.1:c.*469C>T | ENSP00000494827.1:n.*469C>T | |
| ENST00000642772.1:c.*94+5834C>T | ENSP00000495041.1:n.*94+5834C>T | |
| ENST00000643042.1:c.518C>T | ENSP00000496674.1:n.518C>T | |
| ENST00000643619.1:c.*480C>T | ENSP00000494378.1:n.*480C>T | |
| ENST00000643752.1:c.*223C>T | ENSP00000495000.1:n.*223C>T | |
| ENST00000644088.1:c.*218C>T | ENSP00000494066.1:n.*218C>T | |
| ENST00000644591.1:c.*223C>T | ENSP00000496664.1:n.*223C>T | |
| ENST00000644895.1:c.*99+5834C>T | ENSP00000493872.1:n.*99+5834C>T | |
| ENST00000645345.1:c.*469C>T | ENSP00000495859.1:n.*469C>T | |
| ENST00000647524.1:c.*480C>T | ENSP00000495077.1:n.*480C>T | |
| ENST00000373189.5:c.897C>T | ENSP00000362285.5:p.Arg299= | |
| ENST00000469204.1:n.394C>T | ||
| NM_001174098.1:c.*126C>T | NP_001167569.1:n.*126C>T | |
| NM_018344.5:c.897C>T | NP_060814.4:p.Arg299= | |
| NR_033413.1:n.871C>T | ||
| NR_033414.1:n.644C>T | ||
| XM_006717910.2:c.663C>T | XP_006717973.1:p.Arg221= | |
| NM_001363518.1:c.663C>T | NP_001350447.1:p.Arg221= | |
| XM_017016377.2:c.459C>T | XP_016871866.1:p.Arg153= | |
| XM_017016378.2:c.279C>T | XP_016871867.1:p.Arg93= | |
| NM_018344.6:c.897C>T MANE Select | NP_060814.4:p.Arg299= | |
| NM_001174098.2:c.*126C>T | NP_001167569.1:n.*126C>T | |
| NM_001363518.2:c.663C>T | NP_001350447.1:p.Arg221= | |
| NR_033413.2:n.865C>T | ||
| NR_033414.2:n.638C>T |