Linked Data
MyVariant Identifiers:
chr14:g.50088742T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.49622024T>A , CM000676.2:g.49622024T>A | GRCh38 |
| NC_000014.8:g.50088742T>A , CM000676.1:g.50088742T>A | GRCh37 |
| NC_000014.7:g.49158492T>A | NCBI36 |
| NG_008920.1:g.6254T>A | |
| NG_033054.1:g.3608A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305386.4:c.756T>A MANE Select | ENSP00000307423.2:p.Ala252= | |
| ENST00000305386.3:c.756T>A | ENSP00000307423.2:p.Ala252= | |
| NM_002408.3:c.756T>A | NP_002399.1:p.Ala252= | |
| NM_002408.4:c.756T>A MANE Select | NP_002399.1:p.Ala252= |