Linked Data
ClinVar Variation Id:
793236
ClinVar RCV Id:
RCV000976409
dbSNP Id:
rs75166536
ExAC:
10:50690805 C / T
gnomAD v2:
10-50690805-C-T
gnomAD v3:
10-49482759-C-T
gnomAD v4:
10-49482759-C-T
COSMIC:
COSM2145461
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.49482759C>T , CM000672.2:g.49482759C>T | GRCh38 |
| NC_000010.10:g.50690805C>T , CM000672.1:g.50690805C>T | GRCh37 |
| NC_000010.9:g.50360811C>T | NCBI36 |
| NG_009442.1:g.61343G>A , LRG_465:g.61343G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000355832.10:c.2097G>A MANE Select | ENSP00000348089.5:p.Thr699= | |
| ENST00000681632.1:n.2175G>A | ||
| ENST00000681659.1:c.1938G>A | ENSP00000505631.1:p.Thr646= | |
| ENST00000355832.9:c.2097G>A | ENSP00000348089.5:p.Thr699= | |
| ENST00000623073.3:c.*489G>A | ENSP00000485650.1:n.*489G>A | |
| ENST00000623115.3:c.207G>A | ENSP00000485321.1:p.Thr69= | |
| NM_000124.3:c.2097G>A | NP_000115.1:p.Thr699= | |
| NM_001346440.1:c.2097G>A | NP_001333369.1:p.Thr699= | |
| NM_000124.4:c.2097G>A MANE Select | NP_000115.1:p.Thr699= | |
| NM_001346440.2:c.2097G>A | NP_001333369.1:p.Thr699= |