Linked Data
ClinVar Variation Id:
1210034
dbSNP Id:
rs111833428
ExAC:
19:45411042 G / A
gnomAD v2:
19-45411042-G-A
gnomAD v3:
19-44907785-G-A
gnomAD v4:
19-44907785-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.44907785G>A , CM000681.2:g.44907785G>A | GRCh38 |
| NC_000019.9:g.45411042G>A , CM000681.1:g.45411042G>A | GRCh37 |
| NC_000019.8:g.50102882G>A | NCBI36 |
| NG_007084.2:g.7004G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252486.9:c.69G>A MANE Select | ENSP00000252486.3:p.Ala23= | |
| ENST00000252486.8:c.69G>A | ENSP00000252486.3:p.Ala23= | |
| ENST00000425718.1:c.69G>A | ENSP00000410423.1:p.Ala23= | |
| ENST00000434152.5:c.147G>A | ENSP00000413653.2:p.Ala49= | |
| ENST00000446996.5:c.69G>A | ENSP00000413135.1:p.Ala23= | |
| NM_000041.3:c.69G>A | NP_000032.1:p.Ala23= | |
| NM_001302688.1:c.147G>A | NP_001289617.1:p.Ala49= | |
| NM_001302689.1:c.69G>A | NP_001289618.1:p.Ala23= | |
| NM_001302690.1:c.69G>A | NP_001289619.1:p.Ala23= | |
| NM_001302691.1:c.69G>A | NP_001289620.1:p.Ala23= | |
| NM_000041.4:c.69G>A MANE Select | NP_000032.1:p.Ala23= | |
| NM_001302688.2:c.147G>A | NP_001289617.1:p.Ala49= | |
| NM_001302689.2:c.69G>A | NP_001289618.1:p.Ala23= | |
| NM_001302691.2:c.69G>A | NP_001289620.1:p.Ala23= | |
| NM_001302690.2:c.69G>A | NP_001289619.1:p.Ala23= |