Linked Data
MyVariant Identifiers:
chr8:g.6735320T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.6877798T>C , CM000670.2:g.6877798T>C | GRCh38 |
| NC_000008.10:g.6735320T>C , CM000670.1:g.6735320T>C | GRCh37 |
| NC_000008.9:g.6722730T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000297439.4:c.60A>G MANE Select | ENSP00000297439.3:p.Ser20= | |
| ENST00000297439.3:c.60A>G | ENSP00000297439.3:p.Ser20= | |
| NM_005218.3:c.60A>G | NP_005209.1:p.Ser20= | |
| NM_005218.4:c.60A>G MANE Select | NP_005209.1:p.Ser20= |