Linked Data
MyVariant Identifiers:
chr14:g.50597298T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50130580T>A , CM000676.2:g.50130580T>A | GRCh38 |
| NC_000014.8:g.50597298T>A , CM000676.1:g.50597298T>A | GRCh37 |
| NC_000014.7:g.49667048T>A | NCBI36 |
| NG_051073.1:g.106114A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216373.10:c.3258A>T MANE Select | ENSP00000216373.5:p.Pro1086= | |
| ENST00000216373.9:c.3258A>T | ENSP00000216373.5:p.Pro1086= | |
| ENST00000543680.5:c.3159A>T | ENSP00000445328.1:p.Pro1053= | |
| NM_006939.2:c.3258A>T | NP_008870.2:p.Pro1086= | |
| XM_005268021.1:c.3078A>T | XP_005268078.1:p.Pro1026= | |
| XM_011537103.1:c.3219A>T | XP_011535405.1:p.Pro1073= | |
| NM_006939.3:c.3258A>T | NP_008870.2:p.Pro1086= | |
| NM_006939.4:c.3258A>T MANE Select | NP_008870.2:p.Pro1086= |