Linked Data
ClinVar Variation Id:
1450057
ClinVar RCV Id:
RCV001989950
dbSNP Id:
rs71532874
gnomAD v2:
4-6304133-G-C
gnomAD v3:
4-6302406-G-C
gnomAD v4:
4-6302406-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.6302406G>C , CM000666.2:g.6302406G>C | GRCh38 |
| NC_000004.11:g.6304133G>C , CM000666.1:g.6304133G>C | GRCh37 |
| NC_000004.10:g.6355034G>C | NCBI36 |
| NG_011700.1:g.37557G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682275.1:c.2647G>C | ENSP00000507852.1:p.Val883Leu | |
| ENST00000683395.1:c.2588G>C | ||
| ENST00000684087.1:c.2611G>C | ENSP00000506978.1:p.Val871Leu | |
| ENST00000506362.2:c.2362G>C | ENSP00000424103.2:p.Val788Leu | |
| ENST00000673991.1:c.2647G>C | ENSP00000501033.1:p.Val883Leu | |
| ENST00000226760.5:c.2611G>C MANE Select | ENSP00000226760.1:p.Val871Leu | |
| ENST00000503569.5:c.2611G>C | ENSP00000423337.1:p.Val871Leu | |
| ENST00000507765.1:n.2796G>C | ||
| NM_001145853.1:c.2611G>C | NP_001139325.1:p.Val871Leu | |
| NM_006005.3:c.2611G>C MANE Select | NP_005996.2:p.Val871Leu | |
| XM_017008586.1:c.2620G>C | XP_016864075.1:p.Val874Leu |