Linked Data
MyVariant Identifiers:
chr10:g.96748779T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94989022T>A , CM000672.2:g.94989022T>A | GRCh38 |
| NC_000010.10:g.96748779T>A , CM000672.1:g.96748779T>A | GRCh37 |
| NC_000010.9:g.96738769T>A | NCBI36 |
| NG_008385.1:g.55365T>A | |
| NG_008385.2:g.55865T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260682.8:c.1467T>A MANE Select | ENSP00000260682.6:p.Pro489= | |
| ENST00000643112.1:c.*476T>A | ENSP00000496202.1:n.*476T>A | |
| ENST00000260682.6:c.1467T>A | ENSP00000260682.6:p.Pro489= | |
| NM_000771.3:c.1467T>A | NP_000762.2:p.Pro489= | |
| NM_000771.4:c.1467T>A MANE Select | NP_000762.2:p.Pro489= |