Linked Data
MyVariant Identifiers:
chr4:g.4864441C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.4862714C>A , CM000666.2:g.4862714C>A | GRCh38 |
| NC_000004.11:g.4864441C>A , CM000666.1:g.4864441C>A | GRCh37 |
| NC_000004.10:g.4915342C>A | NCBI36 |
| NG_008121.1:g.8050C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382723.5:c.483C>A MANE Select | ENSP00000372170.4:p.Pro161= | |
| ENST00000382723.4:c.483C>A | ENSP00000372170.4:p.Pro161= | |
| ENST00000468421.1:n.195C>A | ||
| NM_002448.3:c.483C>A MANE Select | NP_002439.2:p.Pro161= |