Linked Data
MyVariant Identifiers:
chr15:g.74631948G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74339607G>C , CM000677.2:g.74339607G>C | GRCh38 |
| NC_000015.9:g.74631948G>C , CM000677.1:g.74631948G>C | GRCh37 |
| NC_000015.8:g.72419001G>C | NCBI36 |
| NG_007973.1:g.33135C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268053.11:c.1137C>G MANE Select | ENSP00000268053.6:p.Ala379= | |
| ENST00000268053.10:c.1137C>G | ENSP00000268053.6:p.Ala379= | |
| ENST00000358632.8:c.663C>G | ENSP00000351455.4:p.Ala221= | |
| ENST00000435365.5:c.1137C>G | ENSP00000391081.1:p.Ala379= | |
| ENST00000566674.5:c.663C>G | ENSP00000456941.1:p.Ala221= | |
| NM_000781.2:c.1137C>G | NP_000772.2:p.Ala379= | |
| NM_001099773.1:c.663C>G | NP_001093243.1:p.Ala221= | |
| NM_000781.3:c.1137C>G MANE Select | NP_000772.2:p.Ala379= | |
| NM_001099773.2:c.663C>G | NP_001093243.1:p.Ala221= |