Linked Data
dbSNP Id:
rs1730963051
gnomAD v4:
4-6302189-C-G
MyVariant Identifiers:
chr4:g.6303916C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.6302189C>G , CM000666.2:g.6302189C>G | GRCh38 |
| NC_000004.11:g.6303916C>G , CM000666.1:g.6303916C>G | GRCh37 |
| NC_000004.10:g.6354817C>G | NCBI36 |
| NG_011700.1:g.37340C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000682275.1:c.2430C>G | ENSP00000507852.1:p.Val810= | |
| ENST00000683395.1:c.2371C>G | ||
| ENST00000684087.1:c.2394C>G | ENSP00000506978.1:p.Val798= | |
| ENST00000506362.2:c.2145C>G | ENSP00000424103.2:p.Val715= | |
| ENST00000673991.1:c.2430C>G | ENSP00000501033.1:p.Val810= | |
| ENST00000226760.5:c.2394C>G MANE Select | ENSP00000226760.1:p.Val798= | |
| ENST00000503569.5:c.2394C>G | ENSP00000423337.1:p.Val798= | |
| ENST00000507765.1:n.2579C>G | ||
| NM_001145853.1:c.2394C>G | NP_001139325.1:p.Val798= | |
| NM_006005.3:c.2394C>G MANE Select | NP_005996.2:p.Val798= | |
| XM_017008586.1:c.2403C>G | XP_016864075.1:p.Val801= |