Linked Data
ClinVar Variation Id:
2843522
ClinVar RCV Id:
RCV003723978
gnomAD v4:
19-36006615-G-A
MyVariant Identifiers:
chr19:g.36497517G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.36006615G>A , CM000681.2:g.36006615G>A | GRCh38 |
| NC_000019.9:g.36497517G>A , CM000681.1:g.36497517G>A | GRCh37 |
| NC_000019.8:g.41189357G>A | NCBI36 |
| NG_042831.1:g.7179C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000324444.9:c.675C>T MANE Select | ENSP00000316130.3:p.Asp225= | |
| ENST00000397428.8:c.67-1178C>T | ||
| ENST00000465425.2:n.787C>T | ||
| ENST00000324444.7:c.675C>T | ENSP00000316130.3:p.Asp225= | |
| ENST00000340477.9:c.336C>T | ENSP00000343152.5:p.Asp112= | |
| ENST00000397428.7:c.40-1178C>T | ENSP00000380572.3:n.40-1178C>T | |
| ENST00000465425.1:n.787C>T | ||
| ENST00000490730.1:c.675C>T | ENSP00000422716.1:p.Asp225= | |
| ENST00000503121.5:c.242+1602C>T | ||
| ENST00000505054.2:n.395-1178C>T | ||
| NM_001039876.1:c.675C>T | NP_001034965.1:p.Asp225= | |
| NM_001039876.2:c.675C>T | NP_001034965.1:p.Asp225= | |
| NM_001297735.1:c.336C>T | NP_001284664.1:p.Asp112= | |
| NM_001297735.2:c.336C>T | NP_001284664.1:p.Asp112= | |
| XM_005258598.2:c.675C>T | XP_005258655.1:p.Asp225= | |
| XM_005258601.2:c.618+135C>T | XP_005258658.1:n.618+135C>T | |
| XM_005258604.3:c.675C>T | XP_005258661.1:p.Asp225= | |
| NM_001039876.3:c.675C>T MANE Select | NP_001034965.1:p.Asp225= | |
| NM_001297735.3:c.336C>T | NP_001284664.1:p.Asp112= |