Linked Data
ClinVar Variation Id:
1930060
ClinVar RCV Id:
RCV002626623
MyVariant Identifiers:
chr8:g.37623240G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37765722G>A , CM000670.2:g.37765722G>A | GRCh38 |
| NC_000008.10:g.37623240G>A , CM000670.1:g.37623240G>A | GRCh37 |
| NC_000008.9:g.37742398G>A | NCBI36 |
| NG_053030.1:g.8970G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000328195.8:c.219G>A MANE Select | ENSP00000333551.3:p.Leu73= | |
| ENST00000328195.7:c.219G>A | ENSP00000333551.3:p.Leu73= | |
| ENST00000518036.5:c.*71G>A | ENSP00000428005.1:n.*71G>A | |
| ENST00000520073.5:n.284G>A | ||
| ENST00000523187.5:c.63G>A | ENSP00000427886.1:p.Leu21= | |
| ENST00000523358.5:c.219G>A | ENSP00000427778.1:p.Leu73= | |
| ENST00000523994.1:n.224G>A | ||
| NM_007198.3:c.219G>A | NP_009129.1:p.Leu73= | |
| NM_001349346.1:c.219G>A | NP_001336275.1:p.Leu73= | |
| NM_001349347.1:c.213G>A | NP_001336276.1:p.Leu71= | |
| NM_001349348.1:c.63G>A | NP_001336277.1:p.Leu21= | |
| NM_001349349.1:c.324G>A | NP_001336278.1:p.Leu108= | |
| NM_007198.4:c.219G>A MANE Select | NP_009129.1:p.Leu73= | |
| NM_001349346.2:c.219G>A | NP_001336275.1:p.Leu73= | |
| NM_001349347.2:c.213G>A | NP_001336276.1:p.Leu71= | |
| NM_001349348.2:c.63G>A | NP_001336277.1:p.Leu21= |