Linked Data
MyVariant Identifiers:
chr10:g.89487207T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87727450T>G , CM000672.2:g.87727450T>G | GRCh38 |
| NC_000010.10:g.89487207T>G , CM000672.1:g.89487207T>G | GRCh37 |
| NC_000010.9:g.89477187T>G | NCBI36 |
| NG_012150.1:g.72732T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000456849.2:c.1047T>G MANE Select | ENSP00000406157.1:p.Arg349= | |
| ENST00000361175.8:c.1032T>G | ENSP00000354436.4:p.Arg344= | |
| ENST00000456849.1:c.1047T>G | ENSP00000406157.1:p.Arg349= | |
| NM_001015880.1:c.1047T>G | NP_001015880.1:p.Arg349= | |
| NM_004670.3:c.1032T>G | NP_004661.2:p.Arg344= | |
| NM_001015880.2:c.1047T>G MANE Select | NP_001015880.1:p.Arg349= | |
| NM_004670.4:c.1032T>G | NP_004661.2:p.Arg344= |