Linked Data
MyVariant Identifiers:
chr19:g.10226196G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10115520G>T , CM000681.2:g.10115520G>T | GRCh38 |
| NC_000019.9:g.10226196G>T , CM000681.1:g.10226196G>T | GRCh37 |
| NC_000019.8:g.10087196G>T | NCBI36 |
| NG_047007.1:g.9000G>T | |
| NG_051197.1:g.9405C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253108.9:c.906C>A MANE Select | ENSP00000253108.3:p.Gly302= | |
| ENST00000253108.8:c.906C>A | ENSP00000253108.3:p.Gly302= | |
| ENST00000590158.1:n.925C>A | ||
| ENST00000593054.5:c.300C>A | ENSP00000467187.1:p.Gly100= | |
| NM_003755.3:c.906C>A | NP_003746.2:p.Gly302= | |
| NM_003755.4:c.906C>A | NP_003746.2:p.Gly302= | |
| NM_003755.5:c.906C>A MANE Select | NP_003746.2:p.Gly302= |