Linked Data
MyVariant Identifiers:
chr8:g.87751908A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86739680A>T , CM000670.2:g.86739680A>T | GRCh38 |
| NC_000008.10:g.87751908A>T , CM000670.1:g.87751908A>T | GRCh37 |
| NC_000008.9:g.87821024A>T | NCBI36 |
| NG_016980.1:g.8996T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.186T>A MANE Select | ENSP00000316605.5:p.Ser62= | |
| ENST00000681746.1:c.186T>A | ENSP00000505959.1:p.Ser62= | |
| ENST00000320005.5:c.186T>A | ENSP00000316605.5:p.Ser62= | |
| ENST00000519777.1:n.168T>A | ||
| NM_019098.4:c.186T>A | NP_061971.3:p.Ser62= | |
| NM_019098.5:c.186T>A MANE Select | NP_061971.3:p.Ser62= |