Linked Data
ClinVar Variation Id:
2095810
ClinVar RCV Id:
RCV003012525
MyVariant Identifiers:
chr15:g.48737598C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48445401C>T , CM000677.2:g.48445401C>T | GRCh38 |
| NC_000015.9:g.48737598C>T , CM000677.1:g.48737598C>T | GRCh37 |
| NC_000015.8:g.46524890C>T | NCBI36 |
| NG_008805.2:g.205388G>A , LRG_778:g.205388G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.5892G>A | ENSP00000453958.2:p.Val1964= | |
| ENST00000674301.2:c.5892G>A | ENSP00000501333.2:p.Val1964= | |
| ENST00000684448.1:n.4566G>A | ||
| ENST00000316623.10:c.5892G>A MANE Select | ENSP00000325527.5:p.Val1964= | |
| ENST00000674301.1:c.891G>A | ENSP00000501333.1:p.Val297= | |
| ENST00000316623.9:c.5892G>A | ENSP00000325527.5:p.Val1964= | |
| ENST00000537463.6:c.*1655G>A | ENSP00000440294.2:n.*1655G>A | |
| ENST00000559133.5:c.1199G>A | ||
| ENST00000560820.1:n.12G>A | ||
| NM_000138.4:c.5892G>A , LRG_778t1:c.5892G>A | NP_000129.3:p.Val1964= | |
| NM_000138.5:c.5892G>A MANE Select | NP_000129.3:p.Val1964= |