Linked Data
MyVariant Identifiers:
chr17:g.42449789G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44372421G>C , CM000679.2:g.44372421G>C | GRCh38 |
| NC_000017.10:g.42449789G>C , CM000679.1:g.42449789G>C | GRCh37 |
| NC_000017.9:g.39805315G>C | NCBI36 |
| NG_008331.1:g.22085C>G , LRG_479:g.22085C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262407.6:c.3063C>G MANE Select | ENSP00000262407.5:p.Val1021= | |
| ENST00000648408.1:c.2377C>G | ||
| ENST00000262407.5:c.3063C>G | ENSP00000262407.5:p.Val1021= | |
| ENST00000587295.5:c.256C>G | ||
| ENST00000588098.1:c.40C>G | ||
| NM_000419.3:c.3063C>G , LRG_479t1:c.3063C>G | NP_000410.2:p.Val1021= | |
| XM_011524749.1:c.2961C>G | XP_011523051.1:p.Val987= | |
| XM_011524750.1:c.2946C>G | XP_011523052.1:p.Val982= | |
| NM_000419.4:c.3063C>G | NP_000410.2:p.Val1021= | |
| NM_000419.5:c.3063C>G MANE Select | NP_000410.2:p.Val1021= |