Linked Data
ClinVar Variation Id:
764892
ClinVar RCV Id:
RCV000943259
dbSNP Id:
rs535814124
ExAC:
17:73517972 G / A
gnomAD v2:
17-73517972-G-A
gnomAD v3:
17-75521891-G-A
gnomAD v4:
17-75521891-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.75521891G>A , CM000679.2:g.75521891G>A | GRCh38 |
| NC_000017.10:g.73517972G>A , CM000679.1:g.73517972G>A | GRCh37 |
| NC_000017.9:g.71029567G>A | NCBI36 |
| NG_013041.1:g.10364G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333213.11:c.810G>A MANE Select | ENSP00000327487.6:p.Pro270= | |
| ENST00000434205.8:c.507G>A | ENSP00000406559.4:p.Pro169= | |
| ENST00000545228.3:c.810G>A | ENSP00000438169.3:p.Pro270= | |
| ENST00000579449.2:n.609G>A | ||
| ENST00000580013.6:n.1013G>A | ||
| ENST00000583818.2:c.864G>A | ENSP00000461928.2:n.864G>A | |
| ENST00000679370.1:n.1391G>A | ||
| ENST00000679429.1:c.*268G>A | ENSP00000505403.1:n.*268G>A | |
| ENST00000679443.1:n.879G>A | ||
| ENST00000679782.1:c.810G>A | ENSP00000505995.1:p.Pro270= | |
| ENST00000679919.1:n.879G>A | ||
| ENST00000679928.1:c.*421G>A | ENSP00000506071.1:n.*421G>A | |
| ENST00000680528.1:n.835G>A | ||
| ENST00000680999.1:c.810G>A | ENSP00000504984.1:p.Pro270= | |
| ENST00000681282.1:c.*56G>A | ENSP00000506339.1:n.*56G>A | |
| ENST00000333213.10:c.810G>A | ENSP00000327487.6:p.Pro270= | |
| ENST00000578415.1:c.770G>A | ||
| ENST00000583173.5:c.459-116G>A | ENSP00000463619.1:n.459-116G>A | |
| ENST00000583818.1:c.759G>A | ENSP00000461928.1:n.759G>A | |
| NM_207346.2:c.810G>A | NP_997229.2:p.Pro270= | |
| XM_005257229.2:c.810G>A | XP_005257286.1:p.Pro270= | |
| XM_006721821.2:c.507G>A | XP_006721884.1:p.Pro169= | |
| XM_011524616.1:c.810G>A | XP_011522918.1:p.Pro270= | |
| XM_011524617.1:c.810G>A | XP_011522919.1:p.Pro270= | |
| XM_011524618.1:c.810G>A | XP_011522920.1:p.Pro270= | |
| XR_243646.2:n.840G>A | ||
| XM_005257229.4:c.810G>A | XP_005257286.1:p.Pro270= | |
| XR_243646.4:n.846G>A | ||
| NM_207346.3:c.810G>A MANE Select | NP_997229.2:p.Pro270= |