Linked Data
MyVariant Identifiers:
chr4:g.46125868C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.46123851C>A , CM000666.2:g.46123851C>A | GRCh38 |
| NC_000004.11:g.46125868C>A , CM000666.1:g.46125868C>A | GRCh37 |
| NC_000004.10:g.45820625C>A | NCBI36 |
| NG_046964.1:g.5215G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295452.5:c.63G>T MANE Select | ENSP00000295452.4:p.Val21= | |
| ENST00000295452.4:c.63G>T | ENSP00000295452.4:p.Val21= | |
| NM_173536.3:c.63G>T | NP_775807.2:p.Val21= | |
| NM_173536.4:c.63G>T MANE Select | NP_775807.2:p.Val21= |