Linked Data
ClinVar Variation Id:
421661
ClinVar RCV Id:
RCV000479860
dbSNP Id:
rs1064795279
gnomAD v4:
1-215780042-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215780042C>A , CM000663.2:g.215780042C>A | GRCh38 |
| NC_000001.10:g.215953384C>A , CM000663.1:g.215953384C>A | GRCh37 |
| NC_000001.9:g.214020007C>A | NCBI36 |
| NG_009497.1:g.648355G>T | |
| NG_009497.2:g.648407G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.10741-1G>T MANE Select | ENSP00000305941.3:n.10741-1G>T | |
| ENST00000674083.1:c.10741-1G>T | ENSP00000501296.1:n.10741-1G>T | |
| ENST00000307340.7:c.10741-1G>T | ENSP00000305941.3:n.10741-1G>T | |
| NM_206933.2:c.10741-1G>T | NP_996816.2:n.10741-1G>T | |
| NM_206933.3:c.10741-1G>T | NP_996816.2:n.10741-1G>T | |
| NM_206933.4:c.10741-1G>T MANE Select | NP_996816.3:n.10741-1G>T |