Linked Data
MyVariant Identifiers:
chr10:g.82034953C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.80275197C>T , CM000672.2:g.80275197C>T | GRCh38 |
| NC_000010.10:g.82034953C>T , CM000672.1:g.82034953C>T | GRCh37 |
| NC_000010.9:g.82024933C>T | NCBI36 |
| NG_008083.1:g.19482G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372213.8:c.771G>A MANE Select | ENSP00000361287.3:p.Gly257= | |
| ENST00000372213.7:c.771G>A | ENSP00000361287.3:p.Gly257= | |
| ENST00000480845.1:n.3G>A | ||
| ENST00000485270.5:n.283G>A | ||
| NM_000429.2:c.771G>A | NP_000420.1:p.Gly257= | |
| XM_005269842.3:c.771G>A | XP_005269899.1:p.Gly257= | |
| XM_005269843.3:c.648G>A | XP_005269900.1:p.Gly216= | |
| NM_000429.3:c.771G>A MANE Select | NP_000420.1:p.Gly257= |