Linked Data
ClinVar Variation Id:
1517245
ClinVar RCV Id:
RCV002027208
dbSNP Id:
rs1187025942
COSMIC:
COSM97029
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29220749C>T , CM000664.2:g.29220749C>T | GRCh38 |
| NC_000002.11:g.29443615C>T , CM000664.1:g.29443615C>T | GRCh37 |
| NC_000002.10:g.29297119C>T | NCBI36 |
| NG_009445.1:g.705818G>A , LRG_488:g.705818G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389048.8:c.3602G>A MANE Select | ENSP00000373700.3:p.Gly1201Glu | |
| ENST00000431873.6:c.829G>A | ||
| ENST00000638605.1:n.479G>A | ||
| ENST00000642122.1:c.398G>A | ENSP00000493203.1:p.Gly133Glu | |
| ENST00000389048.7:c.3602G>A | ENSP00000373700.3:p.Gly1201Glu | |
| ENST00000431873.5:c.482G>A | ENSP00000414027.2:p.Gly161Glu | |
| ENST00000618119.4:c.2471G>A | ENSP00000482733.1:p.Gly824Glu | |
| NM_004304.4:c.3602G>A | NP_004295.2:p.Gly1201Glu | |
| NM_001353765.1:c.398G>A | NP_001340694.1:p.Gly133Glu | |
| XM_024452778.1:c.755G>A | XP_024308546.1:p.Gly252Glu | |
| XM_024452779.1:c.398G>A | XP_024308547.1:p.Gly133Glu | |
| NM_004304.5:c.3602G>A MANE Select | NP_004295.2:p.Gly1201Glu | |
| NM_001353765.2:c.398G>A | NP_001340694.1:p.Gly133Glu |