Linked Data
ClinVar Variation Id:
240155
dbSNP Id:
rs370176106
ExAC:
18:48584806 C / T
gnomAD v2:
18-48584806-C-T
gnomAD v3:
18-51058436-C-T
gnomAD v4:
18-51058436-C-T
COSMIC:
COSM988904
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.51058436C>T , CM000680.2:g.51058436C>T | GRCh38 |
| NC_000018.9:g.48584806C>T , CM000680.1:g.48584806C>T | GRCh37 |
| NC_000018.8:g.46838804C>T | NCBI36 |
| NG_013013.2:g.95397C>T , LRG_318:g.95397C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000588860.6:c.884C>T | ENSP00000465878.2:p.Pro295Leu | |
| ENST00000589076.6:c.884C>T | ENSP00000466934.2:p.Pro295Leu | |
| ENST00000589941.2:c.884C>T | ENSP00000465874.2:p.Pro295Leu | |
| ENST00000590061.2:c.884C>T | ENSP00000464772.2:p.Pro295Leu | |
| ENST00000593223.2:c.884C>T | ENSP00000466118.2:p.Pro295Leu | |
| ENST00000611848.2:c.884C>T | ENSP00000478613.2:p.Pro295Leu | |
| ENST00000684953.1:n.2256C>T | ||
| ENST00000685232.1:n.992C>T | ||
| ENST00000688307.1:n.156-1430C>T | ||
| ENST00000688574.1:n.992C>T | ||
| ENST00000688903.1:n.1098C>T | ||
| ENST00000690892.1:n.992C>T | ||
| ENST00000342988.8:c.884C>T MANE Select | ENSP00000341551.3:p.Pro295Leu | |
| ENST00000342988.7:c.884C>T | ENSP00000341551.3:p.Pro295Leu | |
| ENST00000398417.6:c.884C>T | ENSP00000381452.1:p.Pro295Leu | |
| ENST00000588745.5:c.667+3443C>T | ENSP00000464901.1:n.667+3443C>T | |
| ENST00000591126.5:n.2885C>T | ||
| ENST00000592186.5:c.884C>T | ENSP00000468611.1:p.Pro295Leu | |
| ENST00000611848.1:c.84C>T | ||
| NM_005359.5:c.884C>T , LRG_318t1:c.884C>T | NP_005350.1:p.Pro295Leu | |
| NM_005359.6:c.884C>T MANE Select | NP_005350.1:p.Pro295Leu |