Linked Data
MyVariant Identifiers:
chr1:g.116275570A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115732949A>G , CM000663.2:g.115732949A>G | GRCh38 |
| NC_000001.10:g.116275570A>G , CM000663.1:g.116275570A>G | GRCh37 |
| NC_000001.9:g.116077093A>G | NCBI36 |
| NG_008802.1:g.40857T>C , LRG_404:g.40857T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000488931.2:c.282T>C | ENSP00000518226.1:p.Ala94= | |
| ENST00000261448.6:c.558T>C MANE Select | ENSP00000261448.5:p.Ala186= | |
| ENST00000261448.5:c.558T>C | ENSP00000261448.5:p.Ala186= | |
| NM_001232.3:c.558T>C , LRG_404t1:c.558T>C | NP_001223.2:p.Ala186= | |
| NM_001232.4:c.558T>C MANE Select | NP_001223.2:p.Ala186= |