Linked Data
MyVariant Identifiers:
chr1:g.229568105G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.229432358G>C , CM000663.2:g.229432358G>C | GRCh38 |
| NC_000001.10:g.229568105G>C , CM000663.1:g.229568105G>C | GRCh37 |
| NC_000001.9:g.227634728G>C | NCBI36 |
| NG_006672.1:g.6739C>G , LRG_429:g.6739C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000366683.4:c.528C>G | ENSP00000355644.4:p.Ala176= | |
| ENST00000684723.1:c.393C>G | ENSP00000508084.1:p.Ala131= | |
| ENST00000366683.3:c.479+49C>G | ENSP00000355644.3:n.479+49C>G | |
| ENST00000366684.7:c.528C>G MANE Select | ENSP00000355645.3:p.Ala176= | |
| NM_001100.3:c.528C>G , LRG_429t1:c.528C>G | NP_001091.1:p.Ala176= | |
| NM_001100.4:c.528C>G MANE Select | NP_001091.1:p.Ala176= |