Linked Data
MyVariant Identifiers:
chr4:g.4864612A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.4862885A>C , CM000666.2:g.4862885A>C | GRCh38 |
| NC_000004.11:g.4864612A>C , CM000666.1:g.4864612A>C | GRCh37 |
| NC_000004.10:g.4915513A>C | NCBI36 |
| NG_008121.1:g.8221A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382723.5:c.654A>C MANE Select | ENSP00000372170.4:p.Ile218= | |
| ENST00000382723.4:c.654A>C | ENSP00000372170.4:p.Ile218= | |
| ENST00000468421.1:n.366A>C | ||
| NM_002448.3:c.654A>C MANE Select | NP_002439.2:p.Ile218= |