Linked Data
MyVariant Identifiers:
chr16:g.67974236T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67940333T>G , CM000678.2:g.67940333T>G | GRCh38 |
| NC_000016.9:g.67974236T>G , CM000678.1:g.67974236T>G | GRCh37 |
| NC_000016.8:g.66531737T>G | NCBI36 |
| NG_009778.1:g.8780A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264005.10:c.894A>C MANE Select | ENSP00000264005.5:p.Thr298= | |
| ENST00000264005.9:c.894A>C | ENSP00000264005.5:p.Thr298= | |
| ENST00000570369.5:c.156-259A>C | ||
| ENST00000570980.1:c.678A>C | ENSP00000464651.1:p.Thr226= | |
| ENST00000573538.5:c.632A>C | ENSP00000463220.1:n.632A>C | |
| NM_000229.1:c.894A>C | NP_000220.1:p.Thr298= | |
| NM_000229.2:c.894A>C MANE Select | NP_000220.1:p.Thr298= |