Linked Data
MyVariant Identifiers:
chr1:g.116311094A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115768473A>G , CM000663.2:g.115768473A>G | GRCh38 |
| NC_000001.10:g.116311094A>G , CM000663.1:g.116311094A>G | GRCh37 |
| NC_000001.9:g.116112617A>G | NCBI36 |
| NG_008802.1:g.5333T>C , LRG_404:g.5333T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000488931.2:c.-208T>C | ENSP00000518226.1:n.-208T>C | |
| ENST00000261448.6:c.69T>C MANE Select | ENSP00000261448.5:p.Leu23= | |
| ENST00000261448.5:c.69T>C | ENSP00000261448.5:p.Leu23= | |
| NM_001232.3:c.69T>C , LRG_404t1:c.69T>C | NP_001223.2:p.Leu23= | |
| NM_001232.4:c.69T>C MANE Select | NP_001223.2:p.Leu23= |