Linked Data
MyVariant Identifiers:
chr10:g.112349650C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110589892C>T , CM000672.2:g.110589892C>T | GRCh38 |
| NC_000010.10:g.112349650C>T , CM000672.1:g.112349650C>T | GRCh37 |
| NC_000010.9:g.112339640C>T | NCBI36 |
| NG_012217.1:g.27202C>T , LRG_774:g.27202C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684797.1:n.1310C>T | ||
| ENST00000684988.1:n.2055C>T | ||
| ENST00000687823.1:n.1324C>T | ||
| ENST00000689932.1:n.3473C>T | ||
| ENST00000691297.1:n.1543C>T | ||
| ENST00000691527.1:n.2213C>T | ||
| ENST00000692792.1:n.1529C>T | ||
| ENST00000361804.5:c.1410C>T MANE Select | ENSP00000354720.5:p.Asn470= | |
| ENST00000361804.4:c.1410C>T | ENSP00000354720.4:p.Asn470= | |
| NM_005445.3:c.1410C>T , LRG_774t1:c.1410C>T | NP_005436.1:p.Asn470= | |
| NM_005445.4:c.1410C>T MANE Select | NP_005436.1:p.Asn470= |