Linked Data
ClinVar Variation Id:
1191769
ClinVar RCV Id:
RCV001552966
dbSNP Id:
rs887436159
gnomAD v2:
7-107330625-G-A
gnomAD v4:
7-107690180-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107690180G>A , CM000669.2:g.107690180G>A | GRCh38 |
| NC_000007.13:g.107330625G>A , CM000669.1:g.107330625G>A | GRCh37 |
| NC_000007.12:g.107117861G>A | NCBI36 |
| NG_008489.1:g.34546G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644269.2:c.1206G>A MANE Select | ENSP00000494017.1:p.Val402= | |
| ENST00000265715.7:c.1206G>A | ENSP00000265715.3:p.Val402= | |
| NM_000441.1:c.1206G>A | NP_000432.1:p.Val402= | |
| XM_005250425.1:c.1206G>A | XP_005250482.1:p.Val402= | |
| XM_006716025.2:c.1206G>A | XP_006716088.1:p.Val402= | |
| XM_005250425.2:c.1206G>A | XP_005250482.1:p.Val402= | |
| XM_006716025.3:c.1206G>A | XP_006716088.1:p.Val402= | |
| XM_017012318.1:c.1206G>A | XP_016867807.1:p.Val402= | |
| NM_000441.2:c.1206G>A MANE Select | NP_000432.1:p.Val402= |