Linked Data
MyVariant Identifiers:
chr10:g.112361402C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110601644C>T , CM000672.2:g.110601644C>T | GRCh38 |
| NC_000010.10:g.112361402C>T , CM000672.1:g.112361402C>T | GRCh37 |
| NC_000010.9:g.112351392C>T | NCBI36 |
| NG_012217.1:g.38954C>T , LRG_774:g.38954C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.4885C>T | ||
| ENST00000685743.1:n.2360C>T | ||
| ENST00000686057.1:n.1003C>T | ||
| ENST00000689321.1:n.1615C>T | ||
| ENST00000689986.1:n.441C>T | ||
| ENST00000361804.5:c.2652C>T MANE Select | ENSP00000354720.5:p.Asp884= | |
| ENST00000361804.4:c.2652C>T | ENSP00000354720.4:p.Asp884= | |
| NM_005445.3:c.2652C>T , LRG_774t1:c.2652C>T | NP_005436.1:p.Asp884= | |
| NM_005445.4:c.2652C>T MANE Select | NP_005436.1:p.Asp884= |