Linked Data
MyVariant Identifiers:
chr7:g.27135295G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.27095676G>C , CM000669.2:g.27095676G>C | GRCh38 |
| NC_000007.13:g.27135295G>C , CM000669.1:g.27135295G>C | GRCh37 |
| NC_000007.12:g.27101820G>C | NCBI36 |
| NG_011813.1:g.5331C>G | |
| NG_033087.1:g.4583G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000643460.2:c.237C>G MANE Select | ENSP00000494260.2:p.Thr79= | |
| ENST00000343060.4:c.237C>G | ENSP00000343246.4:p.Thr79= | |
| ENST00000355633.5:c.237C>G | ENSP00000347851.5:p.Thr79= | |
| NM_005522.4:c.237C>G | NP_005513.1:p.Thr79= | |
| NM_153620.2:c.237C>G | NP_705873.2:p.Thr79= | |
| NM_005522.5:c.237C>G MANE Select | NP_005513.2:p.Thr79= | |
| NM_153620.3:c.237C>G | NP_705873.3:p.Thr79= |