Linked Data
MyVariant Identifiers:
chr15:g.75042220C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74749879C>G , CM000677.2:g.74749879C>G | GRCh38 |
| NC_000015.9:g.75042220C>G , CM000677.1:g.75042220C>G | GRCh37 |
| NC_000015.8:g.72829273C>G | NCBI36 |
| NG_008431.1:g.32338C>G | |
| NG_008431.2:g.32338C>G | |
| NG_061543.1:g.6035C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000343932.5:c.141C>G MANE Select | ENSP00000342007.4:p.Gly47= | |
| ENST00000343932.4:c.141C>G | ENSP00000342007.4:p.Gly47= | |
| NM_000761.4:c.141C>G | NP_000752.2:p.Gly47= | |
| NM_000761.5:c.141C>G MANE Select | NP_000752.2:p.Gly47= |