Linked Data
MyVariant Identifiers:
chr4:g.68619787C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67754069C>T , CM000666.2:g.67754069C>T | GRCh38 |
| NC_000004.11:g.68619787C>T , CM000666.1:g.68619787C>T | GRCh37 |
| NC_000004.10:g.68302382C>T | NCBI36 |
| NG_009293.1:g.7018G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226413.5:c.267G>A MANE Select | ENSP00000226413.5:p.Leu89= | |
| ENST00000226413.4:c.267G>A | ENSP00000226413.4:p.Leu89= | |
| ENST00000420975.2:c.267G>A | ENSP00000397561.2:p.Leu89= | |
| NM_000406.2:c.267G>A | NP_000397.1:p.Leu89= | |
| NM_001012763.1:c.267G>A | NP_001012781.1:p.Leu89= | |
| NM_000406.3:c.267G>A MANE Select | NP_000397.1:p.Leu89= | |
| NM_001012763.2:c.267G>A | NP_001012781.1:p.Leu89= |