Linked Data
MyVariant Identifiers:
chr10:g.112361580C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110601822C>A , CM000672.2:g.110601822C>A | GRCh38 |
| NC_000010.10:g.112361580C>A , CM000672.1:g.112361580C>A | GRCh37 |
| NC_000010.9:g.112351570C>A | NCBI36 |
| NG_012217.1:g.39132C>A , LRG_774:g.39132C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.5063C>A | ||
| ENST00000685743.1:n.2538C>A | ||
| ENST00000686057.1:n.1181C>A | ||
| ENST00000689321.1:n.1793C>A | ||
| ENST00000689986.1:n.619C>A | ||
| ENST00000361804.5:c.2830C>A MANE Select | ENSP00000354720.5:p.Arg944= | |
| ENST00000361804.4:c.2830C>A | ENSP00000354720.4:p.Arg944= | |
| NM_005445.3:c.2830C>A , LRG_774t1:c.2830C>A | NP_005436.1:p.Arg944= | |
| NM_005445.4:c.2830C>A MANE Select | NP_005436.1:p.Arg944= |