Linked Data
ClinVar Variation Id:
3071772
ClinVar RCV Id:
RCV004016266
MyVariant Identifiers:
chr15:g.48777632G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48485435G>T , CM000677.2:g.48485435G>T | GRCh38 |
| NC_000015.9:g.48777632G>T , CM000677.1:g.48777632G>T | GRCh37 |
| NC_000015.8:g.46564924G>T | NCBI36 |
| NG_008805.2:g.165354C>A , LRG_778:g.165354C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.3651C>A | ENSP00000453958.2:p.Gly1217= | |
| ENST00000674301.2:c.3651C>A | ENSP00000501333.2:p.Gly1217= | |
| ENST00000684448.1:n.2325C>A | ||
| ENST00000316623.10:c.3651C>A MANE Select | ENSP00000325527.5:p.Gly1217= | |
| ENST00000316623.9:c.3651C>A | ENSP00000325527.5:p.Gly1217= | |
| ENST00000537463.6:c.637-10785C>A | ENSP00000440294.2:n.637-10785C>A | |
| NM_000138.4:c.3651C>A , LRG_778t1:c.3651C>A | NP_000129.3:p.Gly1217= | |
| NM_000138.5:c.3651C>A MANE Select | NP_000129.3:p.Gly1217= |