Linked Data
MyVariant Identifiers:
chr10:g.105218143G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.103458386G>T , CM000672.2:g.103458386G>T | GRCh38 |
| NC_000010.10:g.105218143G>T , CM000672.1:g.105218143G>T | GRCh37 |
| NC_000010.9:g.105208133G>T | NCBI36 |
| NG_016855.1:g.5506C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329905.6:c.366C>A MANE Select | ENSP00000329926.6:p.Gly122= | |
| ENST00000329905.5:c.366C>A | ENSP00000329926.5:p.Gly122= | |
| NM_001001412.3:c.366C>A | NP_001001412.3:p.Gly122= | |
| NM_001001412.4:c.366C>A MANE Select | NP_001001412.3:p.Gly122= |