Linked Data
MyVariant Identifiers:
chr10:g.112361417A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110601659A>G , CM000672.2:g.110601659A>G | GRCh38 |
| NC_000010.10:g.112361417A>G , CM000672.1:g.112361417A>G | GRCh37 |
| NC_000010.9:g.112351407A>G | NCBI36 |
| NG_012217.1:g.38969A>G , LRG_774:g.38969A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.4900A>G | ||
| ENST00000685743.1:n.2375A>G | ||
| ENST00000686057.1:n.1018A>G | ||
| ENST00000689321.1:n.1630A>G | ||
| ENST00000689986.1:n.456A>G | ||
| ENST00000361804.5:c.2667A>G MANE Select | ENSP00000354720.5:p.Lys889= | |
| ENST00000361804.4:c.2667A>G | ENSP00000354720.4:p.Lys889= | |
| NM_005445.3:c.2667A>G , LRG_774t1:c.2667A>G | NP_005436.1:p.Lys889= | |
| NM_005445.4:c.2667A>G MANE Select | NP_005436.1:p.Lys889= |