Linked Data
ClinVar Variation Id:
879490
ClinVar RCV Id:
RCV001107040
dbSNP Id:
rs775968273
ExAC:
10:115348157 C / T
gnomAD v2:
10-115348157-C-T
gnomAD v3:
10-113588398-C-T
gnomAD v4:
10-113588398-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.113588398C>T , CM000672.2:g.113588398C>T | GRCh38 |
| NC_000010.10:g.115348157C>T , CM000672.1:g.115348157C>T | GRCh37 |
| NC_000010.9:g.115338147C>T | NCBI36 |
| NG_008956.1:g.40380C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351270.4:c.*29C>T MANE Select | ENSP00000277903.4:n.*29C>T | |
| ENST00000351270.3:c.*29C>T | ENSP00000277903.4:n.*29C>T | |
| ENST00000542051.5:c.*29C>T | ENSP00000443283.1:n.*29C>T | |
| NM_001177660.1:c.*29C>T | NP_001171131.1:n.*29C>T | |
| NM_004132.3:c.*29C>T | NP_004123.1:n.*29C>T | |
| NM_001177660.2:c.*29C>T | NP_001171131.1:n.*29C>T | |
| NM_004132.4:c.*29C>T | NP_004123.1:n.*29C>T | |
| NM_004132.5:c.*29C>T MANE Select | NP_004123.1:n.*29C>T | |
| NM_001177660.3:c.*29C>T | NP_001171131.1:n.*29C>T |