Linked Data
MyVariant Identifiers:
chr2:g.86257442G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.86030319G>C , CM000664.2:g.86030319G>C | GRCh38 |
| NC_000002.11:g.86257442G>C , CM000664.1:g.86257442G>C | GRCh37 |
| NC_000002.10:g.86110953G>C | NCBI36 |
| NG_050742.2:g.80837C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263857.11:c.4656C>G MANE Select | ENSP00000263857.6:p.Val1552= | |
| ENST00000263857.10:c.4656C>G | ENSP00000263857.6:p.Val1552= | |
| ENST00000409681.1:c.4473C>G | ENSP00000386300.1:p.Val1491= | |
| NM_015425.3:c.4656C>G | NP_056240.2:p.Val1552= | |
| XM_006711983.2:c.4332C>G | XP_006712046.1:p.Val1444= | |
| NM_015425.5:c.4656C>G | NP_056240.2:p.Val1552= | |
| NM_015425.6:c.4656C>G MANE Select | NP_056240.2:p.Val1552= |