Linked Data
ClinVar Variation Id:
3231846
ClinVar RCV Id:
RCV004518561
MyVariant Identifiers:
chr7:g.117232354T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117592300T>C , CM000669.2:g.117592300T>C | GRCh38 |
| NC_000007.13:g.117232354T>C , CM000669.1:g.117232354T>C | GRCh37 |
| NC_000007.12:g.117019590T>C | NCBI36 |
| NG_016465.4:g.131517T>C , LRG_663:g.131517T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647720.2:c.2133T>C | ENSP00000497673.2:p.Phe711= | |
| ENST00000647978.2:c.*1847T>C | ENSP00000497658.1:n.*1847T>C | |
| ENST00000649781.2:c.1950T>C | ENSP00000497203.1:p.Phe650= | |
| ENST00000685018.2:c.2133T>C | ENSP00000510194.2:p.Phe711= | |
| ENST00000687278.2:c.2133T>C | ENSP00000509593.2:p.Phe711= | |
| ENST00000699585.1:c.2133T>C | ENSP00000514456.1:p.Phe711= | |
| ENST00000699598.1:c.2133T>C | ENSP00000514467.1:p.Phe711= | |
| ENST00000699599.1:c.2133T>C | ENSP00000514468.1:p.Phe711= | |
| ENST00000699600.1:c.2133T>C | ENSP00000514469.1:p.Phe711= | |
| ENST00000699601.1:c.*433T>C | ENSP00000514470.1:n.*433T>C | |
| ENST00000699602.1:c.2133T>C | ENSP00000514471.1:p.Phe711= | |
| ENST00000699604.1:c.*1957T>C | ENSP00000514472.1:n.*1957T>C | |
| ENST00000699605.1:c.1707T>C | ENSP00000514473.1:p.Phe569= | |
| ENST00000003084.11:c.2133T>C MANE Select | ENSP00000003084.6:p.Phe711= | |
| ENST00000647978.1:c.*1847T>C | ENSP00000497658.1:n.*1847T>C | |
| ENST00000648260.1:c.1402-10526T>C | ENSP00000497957.1:n.1402-10526T>C | |
| ENST00000649406.1:c.1950T>C | ENSP00000497965.1:p.Phe650= | |
| ENST00000649781.1:c.1950T>C | ENSP00000497203.1:p.Phe650= | |
| ENST00000003084.10:c.2133T>C | ENSP00000003084.6:p.Phe711= | |
| ENST00000426809.5:c.2043T>C | ENSP00000389119.1:p.Phe681= | |
| NM_000492.3:c.2133T>C , LRG_663t1:c.2133T>C | NP_000483.3:p.Phe711= | |
| XM_011515751.1:c.2223T>C | XP_011514053.1:p.Phe741= | |
| XM_011515752.1:c.2223T>C | XP_011514054.1:p.Phe741= | |
| XM_011515753.1:c.1890T>C | XP_011514055.1:p.Phe630= | |
| XM_011515754.1:c.1890T>C | XP_011514056.1:p.Phe630= | |
| NM_000492.4:c.2133T>C MANE Select | NP_000483.3:p.Phe711= |