Linked Data
ClinVar Variation Id:
2795849
ClinVar RCV Id:
RCV003624767
MyVariant Identifiers:
chr14:g.51372152C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50905434C>T , CM000676.2:g.50905434C>T | GRCh38 |
| NC_000014.8:g.51372152C>T , CM000676.1:g.51372152C>T | GRCh37 |
| NC_000014.7:g.50441902C>T | NCBI36 |
| NG_012796.1:g.44097G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216392.8:c.2502G>A MANE Select | ENSP00000216392.7:p.Lys834= | |
| ENST00000216392.7:c.2502G>A | ENSP00000216392.7:p.Lys834= | |
| ENST00000532462.5:c.2379+2837G>A | ENSP00000431657.1:n.2379+2837G>A | |
| ENST00000544180.6:c.2400G>A | ENSP00000443787.1:p.Lys800= | |
| NM_001163940.1:c.2400G>A | NP_001157412.1:p.Lys800= | |
| NM_002863.4:c.2502G>A | NP_002854.3:p.Lys834= | |
| NM_002863.5:c.2502G>A MANE Select | NP_002854.3:p.Lys834= | |
| NM_001163940.2:c.2400G>A | NP_001157412.1:p.Lys800= |