Linked Data
ClinVar Variation Id:
1799040
ClinVar RCV Id:
RCV002436011
MyVariant Identifiers:
chr7:g.94055767G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94426455G>A , CM000669.2:g.94426455G>A | GRCh38 |
| NC_000007.13:g.94055767G>A , CM000669.1:g.94055767G>A | GRCh37 |
| NC_000007.12:g.93893703G>A | NCBI36 |
| NG_007405.1:g.36895G>A , LRG_2:g.36895G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.3030G>A MANE Select | ENSP00000297268.6:p.Glu1010= | |
| ENST00000297268.10:c.3030G>A | ENSP00000297268.6:p.Glu1010= | |
| ENST00000478215.1:n.589G>A | ||
| ENST00000481570.5:n.3003G>A | ||
| ENST00000620463.1:c.3024G>A | ENSP00000477719.1:p.Glu1008= | |
| NM_000089.3:c.3030G>A , LRG_2t1:c.3030G>A | NP_000080.2:p.Glu1010= | |
| NM_000089.4:c.3030G>A MANE Select | NP_000080.2:p.Glu1010= |