Linked Data
MyVariant Identifiers:
chr19:g.10226205C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10115529C>A , CM000681.2:g.10115529C>A | GRCh38 |
| NC_000019.9:g.10226205C>A , CM000681.1:g.10226205C>A | GRCh37 |
| NC_000019.8:g.10087205C>A | NCBI36 |
| NG_047007.1:g.9009C>A | |
| NG_051197.1:g.9396G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253108.9:c.897G>T MANE Select | ENSP00000253108.3:p.Gly299= | |
| ENST00000253108.8:c.897G>T | ENSP00000253108.3:p.Gly299= | |
| ENST00000590158.1:n.916G>T | ||
| ENST00000593054.5:c.291G>T | ENSP00000467187.1:p.Gly97= | |
| NM_003755.3:c.897G>T | NP_003746.2:p.Gly299= | |
| NM_003755.4:c.897G>T | NP_003746.2:p.Gly299= | |
| NM_003755.5:c.897G>T MANE Select | NP_003746.2:p.Gly299= |