Linked Data
MyVariant Identifiers:
chr5:g.66480008T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.67184180T>G , CM000667.2:g.67184180T>G | GRCh38 |
| NC_000005.9:g.66480008T>G , CM000667.1:g.66480008T>G | GRCh37 |
| NC_000005.8:g.66515764T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256447.5:c.663A>C MANE Select | ENSP00000256447.4:p.Ser221= | |
| NM_005582.2:c.663A>C | NP_005573.2:p.Ser221= | |
| XM_005248504.3:c.624A>C | XP_005248561.1:p.Ser208= | |
| XM_005248504.4:c.624A>C | XP_005248561.1:p.Ser208= | |
| NM_005582.3:c.663A>C MANE Select | NP_005573.2:p.Ser221= |