Linked Data
ClinVar Variation Id:
2759756
ClinVar RCV Id:
RCV003571828
gnomAD v4:
4-6302189-C-T
MyVariant Identifiers:
chr4:g.6303916C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.6302189C>T , CM000666.2:g.6302189C>T | GRCh38 |
| NC_000004.11:g.6303916C>T , CM000666.1:g.6303916C>T | GRCh37 |
| NC_000004.10:g.6354817C>T | NCBI36 |
| NG_011700.1:g.37340C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000682275.1:c.2430C>T | ENSP00000507852.1:p.Val810= | |
| ENST00000683395.1:c.2371C>T | ||
| ENST00000684087.1:c.2394C>T | ENSP00000506978.1:p.Val798= | |
| ENST00000506362.2:c.2145C>T | ENSP00000424103.2:p.Val715= | |
| ENST00000673991.1:c.2430C>T | ENSP00000501033.1:p.Val810= | |
| ENST00000226760.5:c.2394C>T MANE Select | ENSP00000226760.1:p.Val798= | |
| ENST00000503569.5:c.2394C>T | ENSP00000423337.1:p.Val798= | |
| ENST00000507765.1:n.2579C>T | ||
| NM_001145853.1:c.2394C>T | NP_001139325.1:p.Val798= | |
| NM_006005.3:c.2394C>T MANE Select | NP_005996.2:p.Val798= | |
| XM_017008586.1:c.2403C>T | XP_016864075.1:p.Val801= |