Linked Data
MyVariant Identifiers:
chr19:g.10226241G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10115565G>A , CM000681.2:g.10115565G>A | GRCh38 |
| NC_000019.9:g.10226241G>A , CM000681.1:g.10226241G>A | GRCh37 |
| NC_000019.8:g.10087241G>A | NCBI36 |
| NG_047007.1:g.9045G>A | |
| NG_051197.1:g.9360C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253108.9:c.861C>T MANE Select | ENSP00000253108.3:p.Phe287= | |
| ENST00000253108.8:c.861C>T | ENSP00000253108.3:p.Phe287= | |
| ENST00000589454.5:c.837C>T | ENSP00000466860.1:p.Phe279= | |
| ENST00000590158.1:n.880C>T | ||
| ENST00000593054.5:c.255C>T | ENSP00000467187.1:p.Phe85= | |
| NM_003755.3:c.861C>T | NP_003746.2:p.Phe287= | |
| NM_003755.4:c.861C>T | NP_003746.2:p.Phe287= | |
| NM_003755.5:c.861C>T MANE Select | NP_003746.2:p.Phe287= |