Linked Data
ClinVar Variation Id:
312536
ClinVar RCV Id:
RCV000309853
dbSNP Id:
rs533965995
gnomAD v2:
13-93879641-C-T
gnomAD v3:
13-93227388-C-T
gnomAD v4:
13-93227388-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.93227388C>T , CM000675.2:g.93227388C>T | GRCh38 |
| NC_000013.10:g.93879641C>T , CM000675.1:g.93879641C>T | GRCh37 |
| NC_000013.9:g.92677642C>T | NCBI36 |
| NG_011880.1:g.5564C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377047.9:c.-69C>T MANE Select | ENSP00000366246.3:n.-69C>T | |
| ENST00000377047.8:c.-69C>T | ENSP00000366246.3:n.-69C>T | |
| NM_005708.3:c.-69C>T | NP_005699.1:n.-69C>T | |
| NM_005708.4:c.-69C>T | NP_005699.1:n.-69C>T | |
| NM_005708.5:c.-69C>T MANE Select | NP_005699.1:n.-69C>T |