Linked Data
MyVariant Identifiers:
chr4:g.24801527C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.24799905C>A , CM000666.2:g.24799905C>A | GRCh38 |
| NC_000004.11:g.24801527C>A , CM000666.1:g.24801527C>A | GRCh37 |
| NC_000004.10:g.24410625C>A | NCBI36 |
| NG_012213.1:g.9443C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382120.4:c.384C>A MANE Select | ENSP00000371554.3:p.Thr128= | |
| ENST00000382120.3:c.384C>A | ENSP00000371554.3:p.Thr128= | |
| NM_003102.2:c.384C>A | NP_003093.2:p.Thr128= | |
| XR_427488.1:n.574C>A | ||
| NM_003102.3:c.384C>A | NP_003093.2:p.Thr128= | |
| NM_003102.4:c.384C>A MANE Select | NP_003093.2:p.Thr128= |