Linked Data
MyVariant Identifiers:
chr10:g.115804878C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.114045119C>A , CM000672.2:g.114045119C>A | GRCh38 |
| NC_000010.10:g.115804878C>A , CM000672.1:g.115804878C>A | GRCh37 |
| NC_000010.9:g.115794868C>A | NCBI36 |
| NG_012187.1:g.6073C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369295.4:c.987C>A MANE Select | ENSP00000358301.2:p.Ile329= | |
| ENST00000369295.3:c.987C>A | ENSP00000358301.2:p.Ile329= | |
| NM_000684.2:c.987C>A | NP_000675.1:p.Ile329= | |
| NM_000684.3:c.987C>A MANE Select | NP_000675.1:p.Ile329= |