Linked Data
MyVariant Identifiers:
chr4:g.68606258A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67740540A>G , CM000666.2:g.67740540A>G | GRCh38 |
| NC_000004.11:g.68606258A>G , CM000666.1:g.68606258A>G | GRCh37 |
| NC_000004.10:g.68288853A>G | NCBI36 |
| NG_009293.1:g.20547T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226413.5:c.927T>C MANE Select | ENSP00000226413.5:p.Phe309= | |
| ENST00000226413.4:c.927T>C | ENSP00000226413.4:p.Phe309= | |
| ENST00000420975.2:c.799T>C | ENSP00000397561.2:n.799T>C | |
| NM_000406.2:c.927T>C | NP_000397.1:p.Phe309= | |
| NM_001012763.1:c.*49T>C | NP_001012781.1:n.*49T>C | |
| NM_000406.3:c.927T>C MANE Select | NP_000397.1:p.Phe309= | |
| NM_001012763.2:c.*49T>C | NP_001012781.1:n.*49T>C |