Linked Data
MyVariant Identifiers:
chr5:g.66479909T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.67184081T>C , CM000667.2:g.67184081T>C | GRCh38 |
| NC_000005.9:g.66479909T>C , CM000667.1:g.66479909T>C | GRCh37 |
| NC_000005.8:g.66515665T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256447.5:c.762A>G MANE Select | ENSP00000256447.4:p.Thr254= | |
| NM_005582.2:c.762A>G | NP_005573.2:p.Thr254= | |
| XM_005248504.3:c.723A>G | XP_005248561.1:p.Thr241= | |
| XM_005248504.4:c.723A>G | XP_005248561.1:p.Thr241= | |
| NM_005582.3:c.762A>G MANE Select | NP_005573.2:p.Thr254= |