Linked Data
ClinVar Variation Id:
1084787
ClinVar RCV Id:
RCV001401927
dbSNP Id:
rs935617755
gnomAD v2:
13-20763244-G-A
gnomAD v3:
13-20189105-G-A
gnomAD v4:
13-20189105-G-A
COSMIC:
COSM5475716
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.20189105G>A , CM000675.2:g.20189105G>A | GRCh38 |
| NC_000013.10:g.20763244G>A , CM000675.1:g.20763244G>A | GRCh37 |
| NC_000013.9:g.19661244G>A | NCBI36 |
| NG_008358.1:g.8871C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382844.2:c.477C>T | ENSP00000372295.1:p.Asp159= | |
| ENST00000382848.5:c.477C>T MANE Select | ENSP00000372299.4:p.Asp159= | |
| ENST00000382844.1:c.477C>T | ENSP00000372295.1:p.Asp159= | |
| ENST00000382848.4:c.477C>T | ENSP00000372299.4:p.Asp159= | |
| NM_004004.5:c.477C>T | NP_003995.2:p.Asp159= | |
| XM_011535049.1:c.477C>T | XP_011533351.1:p.Asp159= | |
| XM_011535049.2:c.477C>T | XP_011533351.1:p.Asp159= | |
| NM_004004.6:c.477C>T MANE Select | NP_003995.2:p.Asp159= |