Linked Data
MyVariant Identifiers:
chr5:g.66479915C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.67184087C>T , CM000667.2:g.67184087C>T | GRCh38 |
| NC_000005.9:g.66479915C>T , CM000667.1:g.66479915C>T | GRCh37 |
| NC_000005.8:g.66515671C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256447.5:c.756G>A MANE Select | ENSP00000256447.4:p.Leu252= | |
| NM_005582.2:c.756G>A | NP_005573.2:p.Leu252= | |
| XM_005248504.3:c.717G>A | XP_005248561.1:p.Leu239= | |
| XM_005248504.4:c.717G>A | XP_005248561.1:p.Leu239= | |
| NM_005582.3:c.756G>A MANE Select | NP_005573.2:p.Leu252= |