Linked Data
MyVariant Identifiers:
chr7:g.27135169A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.27095550A>T , CM000669.2:g.27095550A>T | GRCh38 |
| NC_000007.13:g.27135169A>T , CM000669.1:g.27135169A>T | GRCh37 |
| NC_000007.12:g.27101694A>T | NCBI36 |
| NG_011813.1:g.5457T>A | |
| NG_033087.1:g.4457A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000643460.2:c.363T>A MANE Select | ENSP00000494260.2:p.Gly121= | |
| ENST00000343060.4:c.363T>A | ENSP00000343246.4:p.Gly121= | |
| ENST00000355633.5:c.354+9T>A | ENSP00000347851.5:n.354+9T>A | |
| NM_005522.4:c.363T>A | NP_005513.1:p.Gly121= | |
| NM_153620.2:c.354+9T>A | NP_705873.2:n.354+9T>A | |
| NM_005522.5:c.363T>A MANE Select | NP_005513.2:p.Gly121= | |
| NM_153620.3:c.354+9T>A | NP_705873.3:n.354+9T>A |