Linked Data
MyVariant Identifiers:
chr7:g.94033894T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94404582T>G , CM000669.2:g.94404582T>G | GRCh38 |
| NC_000007.13:g.94033894T>G , CM000669.1:g.94033894T>G | GRCh37 |
| NC_000007.12:g.93871830T>G | NCBI36 |
| NG_007405.1:g.15022T>G , LRG_2:g.15022T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.306T>G MANE Select | ENSP00000297268.6:p.Pro102= | |
| ENST00000297268.10:c.306T>G | ENSP00000297268.6:p.Pro102= | |
| ENST00000620463.1:c.300T>G | ENSP00000477719.1:p.Pro100= | |
| NM_000089.3:c.306T>G , LRG_2t1:c.306T>G | NP_000080.2:p.Pro102= | |
| NM_000089.4:c.306T>G MANE Select | NP_000080.2:p.Pro102= |