Linked Data
ClinVar Variation Id:
2786638
ClinVar RCV Id:
RCV003762262
MyVariant Identifiers:
chr18:g.48604693T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.51078323T>C , CM000680.2:g.51078323T>C | GRCh38 |
| NC_000018.9:g.48604693T>C , CM000680.1:g.48604693T>C | GRCh37 |
| NC_000018.8:g.46858691T>C | NCBI36 |
| NG_013013.2:g.115284T>C , LRG_318:g.115284T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000588860.6:c.1515T>C | ENSP00000465878.2:p.Phe505= | |
| ENST00000589076.6:c.1515T>C | ENSP00000466934.2:p.Phe505= | |
| ENST00000589941.2:c.1515T>C | ENSP00000465874.2:p.Phe505= | |
| ENST00000590061.2:c.1515T>C | ENSP00000464772.2:p.Phe505= | |
| ENST00000593223.2:c.*1512T>C | ENSP00000466118.2:n.*1512T>C | |
| ENST00000611848.2:c.*167T>C | ENSP00000478613.2:n.*167T>C | |
| ENST00000684953.1:n.3530T>C | ||
| ENST00000685090.1:n.3445T>C | ||
| ENST00000685232.1:n.1736T>C | ||
| ENST00000688574.1:n.1623T>C | ||
| ENST00000691124.1:n.4476T>C | ||
| ENST00000342988.8:c.1515T>C MANE Select | ENSP00000341551.3:p.Phe505= | |
| ENST00000342988.7:c.1515T>C | ENSP00000341551.3:p.Phe505= | |
| ENST00000398417.6:c.1515T>C | ENSP00000381452.1:p.Phe505= | |
| ENST00000586253.1:n.237T>C | ||
| ENST00000588745.5:c.1227T>C | ENSP00000464901.1:p.Phe409= | |
| ENST00000591126.5:n.3516T>C | ||
| ENST00000592186.5:c.1162T>C | ENSP00000468611.1:n.1162T>C | |
| ENST00000611848.1:c.828T>C | ||
| NM_005359.5:c.1515T>C , LRG_318t1:c.1515T>C | NP_005350.1:p.Phe505= | |
| NM_005359.6:c.1515T>C MANE Select | NP_005350.1:p.Phe505= |