Linked Data
MyVariant Identifiers:
chr7:g.17379231C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.17339607C>T , CM000669.2:g.17339607C>T | GRCh38 |
| NC_000007.13:g.17379231C>T , CM000669.1:g.17379231C>T | GRCh37 |
| NC_000007.12:g.17345756C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242057.9:c.1782C>T MANE Select | ENSP00000242057.4:p.Phe594= | |
| ENST00000637807.1:c.1752C>T | ENSP00000490530.1:p.Phe584= | |
| ENST00000642825.1:c.1737C>T | ENSP00000495987.1:p.Phe579= | |
| ENST00000242057.8:c.1782C>T | ENSP00000242057.4:p.Phe594= | |
| ENST00000463496.1:c.1782C>T | ENSP00000436466.1:p.Phe594= | |
| NM_001621.4:c.1782C>T | NP_001612.1:p.Phe594= | |
| NM_001621.5:c.1782C>T MANE Select | NP_001612.1:p.Phe594= |