Linked Data
MyVariant Identifiers:
chr15:g.40764501C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.40472302C>T , CM000677.2:g.40472302C>T | GRCh38 |
| NC_000015.9:g.40764501C>T , CM000677.1:g.40764501C>T | GRCh37 |
| NC_000015.8:g.38551793C>T | NCBI36 |
| NG_017074.1:g.6342C>T , LRG_600:g.6342C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306243.7:c.1089C>T MANE Select | ENSP00000307297.6:p.Ala363= | |
| ENST00000306243.6:c.1089C>T | ENSP00000307297.5:p.Ala363= | |
| ENST00000559991.1:c.1014C>T | ENSP00000453882.1:p.Ala338= | |
| NM_130468.3:c.1089C>T , LRG_600t1:c.1089C>T | NP_569735.1:p.Ala363= | |
| NM_130468.4:c.1089C>T MANE Select | NP_569735.1:p.Ala363= |