Linked Data
ClinVar Variation Id:
1529969
ClinVar RCV Id:
RCV002089476
dbSNP Id:
rs1436342215
gnomAD v4:
3-10142099-G-A
MyVariant Identifiers:
chr3:g.10183783G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10142099G>A , CM000665.2:g.10142099G>A | GRCh38 |
| NC_000003.11:g.10183783G>A , CM000665.1:g.10183783G>A | GRCh37 |
| NC_000003.10:g.10158783G>A | NCBI36 |
| NG_008212.3:g.5465G>A , LRG_322:g.5465G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696142.1:c.252G>A | ENSP00000512434.1:p.Val84= | |
| ENST00000696143.1:c.252G>A | ENSP00000512435.1:p.Val84= | |
| ENST00000696153.1:c.252G>A | ENSP00000512444.1:p.Val84= | |
| ENST00000256474.3:c.252G>A MANE Select | ENSP00000256474.3:p.Val84= | |
| ENST00000256474.2:c.252G>A | ENSP00000256474.2:p.Val84= | |
| ENST00000345392.2:c.252G>A | ENSP00000344757.2:p.Val84= | |
| NM_000551.3:c.252G>A , LRG_322t1:c.252G>A | NP_000542.1:p.Val84= | |
| NM_198156.2:c.252G>A | NP_937799.1:p.Val84= | |
| XM_011534078.1:c.252G>A | XP_011532380.1:p.Val84= | |
| NM_001354723.1:c.252G>A | NP_001341652.1:p.Val84= | |
| NM_000551.4:c.252G>A MANE Select | NP_000542.1:p.Val84= | |
| NM_001354723.2:c.252G>A | NP_001341652.1:p.Val84= | |
| NM_198156.3:c.252G>A | NP_937799.1:p.Val84= |