Linked Data
ClinVar Variation Id:
925388
ClinVar RCV Id:
RCV001187270
dbSNP Id:
rs2043544643
MyVariant Identifiers:
chr15:g.48782226G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48490029G>A , CM000677.2:g.48490029G>A | GRCh38 |
| NC_000015.9:g.48782226G>A , CM000677.1:g.48782226G>A | GRCh37 |
| NC_000015.8:g.46569518G>A | NCBI36 |
| NG_008805.2:g.160760C>T , LRG_778:g.160760C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.2904C>T | ENSP00000453958.2:p.Thr968= | |
| ENST00000674301.2:c.2904C>T | ENSP00000501333.2:p.Thr968= | |
| ENST00000684448.1:n.1578C>T | ||
| ENST00000316623.10:c.2904C>T MANE Select | ENSP00000325527.5:p.Thr968= | |
| ENST00000316623.9:c.2904C>T | ENSP00000325527.5:p.Thr968= | |
| ENST00000537463.6:c.637-15379C>T | ENSP00000440294.2:n.637-15379C>T | |
| NM_000138.4:c.2904C>T , LRG_778t1:c.2904C>T | NP_000129.3:p.Thr968= | |
| NM_000138.5:c.2904C>T MANE Select | NP_000129.3:p.Thr968= |