Linked Data
MyVariant Identifiers:
chr10:g.112337202T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110577444T>C , CM000672.2:g.110577444T>C | GRCh38 |
| NC_000010.10:g.112337202T>C , CM000672.1:g.112337202T>C | GRCh37 |
| NC_000010.9:g.112327192T>C | NCBI36 |
| NG_012217.1:g.14754T>C , LRG_774:g.14754T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.355T>C | ||
| ENST00000687823.1:n.136T>C | ||
| ENST00000689932.1:n.2285T>C | ||
| ENST00000691297.1:n.355T>C | ||
| ENST00000691527.1:n.312T>C | ||
| ENST00000692792.1:n.341T>C | ||
| ENST00000361804.5:c.222T>C MANE Select | ENSP00000354720.5:p.Ile74= | |
| ENST00000361804.4:c.222T>C | ENSP00000354720.4:p.Ile74= | |
| ENST00000462899.1:n.368T>C | ||
| NM_005445.3:c.222T>C , LRG_774t1:c.222T>C | NP_005436.1:p.Ile74= | |
| NM_005445.4:c.222T>C MANE Select | NP_005436.1:p.Ile74= |