Linked Data
ClinVar Variation Id:
379889
dbSNP Id:
rs529500747
ExAC:
13:20763698 G / A
gnomAD v2:
13-20763698-G-A
gnomAD v3:
13-20189559-G-A
gnomAD v4:
13-20189559-G-A
COSMIC:
COSM3744080
ERepo:
CA6904332/MONDO:0019497/005
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.20189559G>A , CM000675.2:g.20189559G>A | GRCh38 |
| NC_000013.10:g.20763698G>A , CM000675.1:g.20763698G>A | GRCh37 |
| NC_000013.9:g.19661698G>A | NCBI36 |
| NG_008358.1:g.8417C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382844.2:c.23C>T | ENSP00000372295.1:p.Thr8Met | |
| ENST00000382848.5:c.23C>T MANE Select | ENSP00000372299.4:p.Thr8Met | |
| ENST00000382844.1:c.23C>T | ENSP00000372295.1:p.Thr8Met | |
| ENST00000382848.4:c.23C>T | ENSP00000372299.4:p.Thr8Met | |
| NM_004004.5:c.23C>T | NP_003995.2:p.Thr8Met | |
| XM_011535049.1:c.23C>T | XP_011533351.1:p.Thr8Met | |
| XM_011535049.2:c.23C>T | XP_011533351.1:p.Thr8Met | |
| NM_004004.6:c.23C>T MANE Select | NP_003995.2:p.Thr8Met |