Linked Data
ClinVar Variation Id:
354809
ClinVar RCV Id:
RCV000261776
dbSNP Id:
rs886060935
gnomAD v2:
6-108189136-C-T
gnomAD v3:
6-107867932-C-T
gnomAD v4:
6-107867932-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.107867932C>T , CM000668.2:g.107867932C>T | GRCh38 |
| NC_000006.11:g.108189136C>T , CM000668.1:g.108189136C>T | GRCh37 |
| NC_000006.10:g.108295829C>T | NCBI36 |
| NG_008270.1:g.95347G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369002.9:c.*3772G>A MANE Select | ENSP00000357998.4:n.*3772G>A | |
| ENST00000369002.8:c.*3772G>A | ENSP00000357998.4:n.*3772G>A | |
| NM_007214.4:c.*3772G>A | NP_009145.1:n.*3772G>A | |
| NM_007214.5:c.*3772G>A MANE Select | NP_009145.1:n.*3772G>A |