Linked Data
MyVariant Identifiers:
chr10:g.112361846A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110602088A>G , CM000672.2:g.110602088A>G | GRCh38 |
| NC_000010.10:g.112361846A>G , CM000672.1:g.112361846A>G | GRCh37 |
| NC_000010.9:g.112351836A>G | NCBI36 |
| NG_012217.1:g.39398A>G , LRG_774:g.39398A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.5248A>G | ||
| ENST00000685743.1:n.2723A>G | ||
| ENST00000686057.1:n.1366A>G | ||
| ENST00000689321.1:n.1978A>G | ||
| ENST00000689986.1:n.804A>G | ||
| ENST00000361804.5:c.3015A>G MANE Select | ENSP00000354720.5:p.Glu1005= | |
| ENST00000361804.4:c.3015A>G | ENSP00000354720.4:p.Glu1005= | |
| NM_005445.3:c.3015A>G , LRG_774t1:c.3015A>G | NP_005436.1:p.Glu1005= | |
| NM_005445.4:c.3015A>G MANE Select | NP_005436.1:p.Glu1005= |