Linked Data
MyVariant Identifiers:
chr10:g.112341685C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110581927C>A , CM000672.2:g.110581927C>A | GRCh38 |
| NC_000010.10:g.112341685C>A , CM000672.1:g.112341685C>A | GRCh37 |
| NC_000010.9:g.112331675C>A | NCBI36 |
| NG_012217.1:g.19237C>A , LRG_774:g.19237C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.685C>A | ||
| ENST00000687823.1:n.466C>A | ||
| ENST00000689932.1:n.2615C>A | ||
| ENST00000691297.1:n.685C>A | ||
| ENST00000691527.1:n.1355C>A | ||
| ENST00000692792.1:n.671C>A | ||
| ENST00000361804.5:c.552C>A MANE Select | ENSP00000354720.5:p.Gly184= | |
| ENST00000361804.4:c.552C>A | ENSP00000354720.4:p.Gly184= | |
| ENST00000462899.1:n.698C>A | ||
| NM_005445.3:c.552C>A , LRG_774t1:c.552C>A | NP_005436.1:p.Gly184= | |
| NM_005445.4:c.552C>A MANE Select | NP_005436.1:p.Gly184= |