Linked Data
ClinVar Variation Id:
376134
dbSNP Id:
rs1057519783
gnomAD v4:
2-29220747-C-T
COSMIC:
COSM144250
CIViC:
CA16602592
PubMed:
PMID:22277784
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29220747C>T , CM000664.2:g.29220747C>T | GRCh38 |
| NC_000002.11:g.29443613C>T , CM000664.1:g.29443613C>T | GRCh37 |
| NC_000002.10:g.29297117C>T | NCBI36 |
| NG_009445.1:g.705820G>A , LRG_488:g.705820G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389048.8:c.3604G>A MANE Select | ENSP00000373700.3:p.Gly1202Arg | |
| ENST00000431873.6:c.831G>A | ||
| ENST00000638605.1:n.481G>A | ||
| ENST00000642122.1:c.400G>A | ENSP00000493203.1:p.Gly134Arg | |
| ENST00000389048.7:c.3604G>A | ENSP00000373700.3:p.Gly1202Arg | |
| ENST00000431873.5:c.484G>A | ENSP00000414027.2:p.Gly162Arg | |
| ENST00000618119.4:c.2473G>A | ENSP00000482733.1:p.Gly825Arg | |
| NM_004304.4:c.3604G>A | NP_004295.2:p.Gly1202Arg | |
| NM_001353765.1:c.400G>A | NP_001340694.1:p.Gly134Arg | |
| XM_024452778.1:c.757G>A | XP_024308546.1:p.Gly253Arg | |
| XM_024452779.1:c.400G>A | XP_024308547.1:p.Gly134Arg | |
| NM_004304.5:c.3604G>A MANE Select | NP_004295.2:p.Gly1202Arg | |
| NM_001353765.2:c.400G>A | NP_001340694.1:p.Gly134Arg |