Linked Data
dbSNP Id:
rs1767260718
gnomAD v3:
6-63984481-G-T
gnomAD v4:
6-63984481-G-T
COSMIC:
COSM1080991
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.63984481G>T , CM000668.2:g.63984481G>T | GRCh38 |
| NC_000006.11:g.64694374G>T , CM000668.1:g.64694374G>T | GRCh37 |
| NC_000006.10:g.64752333G>T | NCBI36 |
| NG_023443.1:g.1727745C>A | |
| NG_023443.2:g.1727745C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000503581.6:c.6957C>A MANE Select | ENSP00000424243.1:p.Phe2319Leu | |
| ENST00000370616.6:c.6957C>A | ENSP00000359650.2:p.Phe2319Leu | |
| ENST00000370618.7:c.6957C>A | ENSP00000359652.4:p.Phe2319Leu | |
| ENST00000370621.7:c.6957C>A | ENSP00000359655.3:p.Phe2319Leu | |
| ENST00000398580.3:c.271C>A | ||
| ENST00000503581.5:c.6957C>A | ENSP00000424243.1:p.Phe2319Leu | |
| NM_001142800.1:c.6957C>A | NP_001136272.1:p.Phe2319Leu | |
| NM_001292009.1:c.6957C>A | NP_001278938.1:p.Phe2319Leu | |
| XR_001744188.1:n.606+16197G>T | ||
| XR_001744189.1:n.129+16197G>T | ||
| XR_001744190.1:n.197+16197G>T | ||
| XR_001744191.1:n.607-1173G>T | ||
| NM_001142800.2:c.6957C>A MANE Select | NP_001136272.1:p.Phe2319Leu | |
| NM_001292009.2:c.6957C>A | NP_001278938.1:p.Phe2319Leu |