Linked Data
MyVariant Identifiers:
chr10:g.112361519A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110601761A>G , CM000672.2:g.110601761A>G | GRCh38 |
| NC_000010.10:g.112361519A>G , CM000672.1:g.112361519A>G | GRCh37 |
| NC_000010.9:g.112351509A>G | NCBI36 |
| NG_012217.1:g.39071A>G , LRG_774:g.39071A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.5002A>G | ||
| ENST00000685743.1:n.2477A>G | ||
| ENST00000686057.1:n.1120A>G | ||
| ENST00000689321.1:n.1732A>G | ||
| ENST00000689986.1:n.558A>G | ||
| ENST00000361804.5:c.2769A>G MANE Select | ENSP00000354720.5:p.Glu923= | |
| ENST00000361804.4:c.2769A>G | ENSP00000354720.4:p.Glu923= | |
| NM_005445.3:c.2769A>G , LRG_774t1:c.2769A>G | NP_005436.1:p.Glu923= | |
| NM_005445.4:c.2769A>G MANE Select | NP_005436.1:p.Glu923= |