Linked Data
MyVariant Identifiers:
chr10:g.69991162A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.68231405A>C , CM000672.2:g.68231405A>C | GRCh38 |
| NC_000010.10:g.69991162A>C , CM000672.1:g.69991162A>C | GRCh37 |
| NC_000010.9:g.69661168A>C | NCBI36 |
| NG_031934.1:g.5709T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373673.5:c.273T>G MANE Select | ENSP00000362777.3:p.Ala91= | |
| ENST00000373673.4:c.273T>G | ENSP00000362777.3:p.Ala91= | |
| NM_145178.3:c.273T>G | NP_660161.1:p.Ala91= | |
| NM_145178.4:c.273T>G MANE Select | NP_660161.1:p.Ala91= |