Linked Data
ClinVar Variation Id:
973860
ClinVar RCV Id:
RCV001250518
dbSNP Id:
rs936934088
gnomAD v4:
7-117603780-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117603780C>T , CM000669.2:g.117603780C>T | GRCh38 |
| NC_000007.13:g.117243834C>T , CM000669.1:g.117243834C>T | GRCh37 |
| NC_000007.12:g.117031070C>T | NCBI36 |
| NG_016465.4:g.142997C>T , LRG_663:g.142997C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647720.2:c.2906C>T | ENSP00000497673.2:p.Ala969Val | |
| ENST00000647978.2:c.*2620C>T | ENSP00000497658.1:n.*2620C>T | |
| ENST00000649781.2:c.2723C>T | ENSP00000497203.1:p.Ala908Val | |
| ENST00000685018.2:c.2906C>T | ENSP00000510194.2:p.Ala969Val | |
| ENST00000687278.2:c.2906C>T | ENSP00000509593.2:p.Ala969Val | |
| ENST00000699585.1:c.2906C>T | ENSP00000514456.1:p.Ala969Val | |
| ENST00000699598.1:c.2906C>T | ENSP00000514467.1:p.Ala969Val | |
| ENST00000699599.1:c.2906C>T | ENSP00000514468.1:p.Ala969Val | |
| ENST00000699600.1:c.2906C>T | ENSP00000514469.1:p.Ala969Val | |
| ENST00000699601.1:c.*1206C>T | ENSP00000514470.1:n.*1206C>T | |
| ENST00000699602.1:c.2906C>T | ENSP00000514471.1:p.Ala969Val | |
| ENST00000699604.1:c.*2730C>T | ENSP00000514472.1:n.*2730C>T | |
| ENST00000699605.1:c.2480C>T | ENSP00000514473.1:p.Ala827Val | |
| ENST00000687278.1:c.497C>T | ENSP00000509593.1:p.Ala166Val | |
| ENST00000003084.11:c.2906C>T MANE Select | ENSP00000003084.6:p.Ala969Val | |
| ENST00000647720.1:c.556C>T | ||
| ENST00000648260.1:c.1688C>T | ENSP00000497957.1:p.Ala563Val | |
| ENST00000649406.1:c.2723C>T | ENSP00000497965.1:p.Ala908Val | |
| ENST00000649781.1:c.2723C>T | ENSP00000497203.1:p.Ala908Val | |
| ENST00000003084.10:c.2906C>T | ENSP00000003084.6:p.Ala969Val | |
| ENST00000426809.5:c.2816C>T | ENSP00000389119.1:p.Ala939Val | |
| NM_000492.3:c.2906C>T , LRG_663t1:c.2906C>T | NP_000483.3:p.Ala969Val | |
| XM_011515751.1:c.2996C>T | XP_011514053.1:p.Ala999Val | |
| XM_011515752.1:c.2996C>T | XP_011514054.1:p.Ala999Val | |
| XM_011515753.1:c.2663C>T | XP_011514055.1:p.Ala888Val | |
| XM_011515754.1:c.2663C>T | XP_011514056.1:p.Ala888Val | |
| NM_000492.4:c.2906C>T MANE Select | NP_000483.3:p.Ala969Val |