Linked Data
ClinVar Variation Id:
354868
ClinVar RCV Id:
RCV000367903
dbSNP Id:
rs557911
gnomAD v2:
6-108191382-A-G
gnomAD v3:
6-107870178-A-G
gnomAD v4:
6-107870178-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.107870178A>G , CM000668.2:g.107870178A>G | GRCh38 |
| NC_000006.11:g.108191382A>G , CM000668.1:g.108191382A>G | GRCh37 |
| NC_000006.10:g.108298075A>G | NCBI36 |
| NG_008270.1:g.93101T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369002.9:c.*1526T>C MANE Select | ENSP00000357998.4:n.*1526T>C | |
| ENST00000369002.8:c.*1526T>C | ENSP00000357998.4:n.*1526T>C | |
| NM_007214.4:c.*1526T>C | NP_009145.1:n.*1526T>C | |
| NM_007214.5:c.*1526T>C MANE Select | NP_009145.1:n.*1526T>C |