Linked Data
MyVariant Identifiers:
chr7:g.5642961C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.5603330C>A , CM000669.2:g.5603330C>A | GRCh38 |
| NC_000007.13:g.5642961C>A , CM000669.1:g.5642961C>A | GRCh37 |
| NC_000007.12:g.5609487C>A | NCBI36 |
| NG_030004.1:g.15526C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382361.8:c.906C>A MANE Select | ENSP00000371798.3:p.Thr302= | |
| ENST00000382361.7:c.906C>A | ENSP00000371798.3:p.Thr302= | |
| ENST00000405801.2:c.72C>A | ENSP00000383982.2:p.Thr24= | |
| ENST00000444748.5:c.72C>A | ENSP00000404506.1:p.Thr24= | |
| ENST00000447103.5:c.72C>A | ENSP00000409967.1:p.Thr24= | |
| ENST00000473330.1:n.459C>A | ||
| NM_003088.3:c.906C>A | NP_003079.1:p.Thr302= | |
| NM_003088.4:c.906C>A MANE Select | NP_003079.1:p.Thr302= |