Linked Data
MyVariant Identifiers:
chr14:g.51372122G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50905404G>T , CM000676.2:g.50905404G>T | GRCh38 |
| NC_000014.8:g.51372122G>T , CM000676.1:g.51372122G>T | GRCh37 |
| NC_000014.7:g.50441872G>T | NCBI36 |
| NG_012796.1:g.44127C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216392.8:c.2532C>A MANE Select | ENSP00000216392.7:p.Val844= | |
| ENST00000216392.7:c.2532C>A | ENSP00000216392.7:p.Val844= | |
| ENST00000532462.5:c.2379+2867C>A | ENSP00000431657.1:n.2379+2867C>A | |
| ENST00000544180.6:c.2430C>A | ENSP00000443787.1:p.Val810= | |
| NM_001163940.1:c.2430C>A | NP_001157412.1:p.Val810= | |
| NM_002863.4:c.2532C>A | NP_002854.3:p.Val844= | |
| NM_002863.5:c.2532C>A MANE Select | NP_002854.3:p.Val844= | |
| NM_001163940.2:c.2430C>A | NP_001157412.1:p.Val810= |