Linked Data
MyVariant Identifiers:
chr5:g.148206406C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.148826843C>A , CM000667.2:g.148826843C>A | GRCh38 |
| NC_000005.9:g.148206406C>A , CM000667.1:g.148206406C>A | GRCh37 |
| NC_000005.8:g.148186599C>A | NCBI36 |
| NG_016421.1:g.5251C>A | |
| NG_016421.2:g.5251C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305988.6:c.12C>A MANE Select | ENSP00000305372.4:p.Pro4= | |
| ENST00000305988.5:c.12C>A | ENSP00000305372.4:p.Pro4= | |
| NM_000024.5:c.12C>A | NP_000015.1:p.Pro4= | |
| NM_000024.6:c.12C>A MANE Select | NP_000015.2:p.Pro4= |