Linked Data
MyVariant Identifiers:
chr17:g.42449774C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44372406C>G , CM000679.2:g.44372406C>G | GRCh38 |
| NC_000017.10:g.42449774C>G , CM000679.1:g.42449774C>G | GRCh37 |
| NC_000017.9:g.39805300C>G | NCBI36 |
| NG_008331.1:g.22100G>C , LRG_479:g.22100G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262407.6:c.3078G>C MANE Select | ENSP00000262407.5:p.Arg1026= | |
| ENST00000648408.1:c.2392G>C | ||
| ENST00000262407.5:c.3078G>C | ENSP00000262407.5:p.Arg1026= | |
| ENST00000587295.5:c.271G>C | ||
| ENST00000588098.1:c.55G>C | ||
| NM_000419.3:c.3078G>C , LRG_479t1:c.3078G>C | NP_000410.2:p.Arg1026= | |
| XM_011524749.1:c.2976G>C | XP_011523051.1:p.Arg992= | |
| XM_011524750.1:c.2961G>C | XP_011523052.1:p.Arg987= | |
| NM_000419.4:c.3078G>C | NP_000410.2:p.Arg1026= | |
| NM_000419.5:c.3078G>C MANE Select | NP_000410.2:p.Arg1026= |