Linked Data
ClinVar Variation Id:
1984527
ClinVar RCV Id:
RCV002756838
dbSNP Id:
rs750486737
ExAC:
17:7127725 G / A
gnomAD v2:
17-7127725-G-A
gnomAD v4:
17-7224406-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7224406G>A , CM000679.2:g.7224406G>A | GRCh38 |
| NC_000017.10:g.7127725G>A , CM000679.1:g.7127725G>A | GRCh37 |
| NC_000017.9:g.7068449G>A | NCBI36 |
| NG_007975.1:g.9573G>A | |
| NG_008391.2:g.645C>T | |
| NG_033038.1:g.15139C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356839.10:c.1605+13G>A MANE Select | ENSP00000349297.5:n.1605+13G>A | |
| ENST00000322910.9:c.*1560+13G>A | ENSP00000325395.5:n.*1560+13G>A | |
| ENST00000350303.9:c.1539+13G>A | ENSP00000344152.5:n.1539+13G>A | |
| ENST00000356839.9:c.1605+13G>A | ENSP00000349297.5:n.1605+13G>A | |
| ENST00000542255.6:c.463+13G>A | ||
| ENST00000543245.6:c.1674+13G>A | ENSP00000438689.2:n.1674+13G>A | |
| ENST00000578319.5:n.113G>A | ||
| ENST00000578711.1:n.902G>A | ||
| ENST00000578809.5:n.177+13G>A | ||
| ENST00000579391.1:n.213+13G>A | ||
| ENST00000579425.5:n.721+13G>A | ||
| ENST00000579546.1:c.344+13G>A | ||
| ENST00000579894.5:n.392+13G>A | ||
| ENST00000582450.1:n.113+13G>A | ||
| ENST00000583074.5:n.226+13G>A | ||
| ENST00000583850.5:n.380+13G>A | ||
| ENST00000583858.5:c.536+13G>A | ||
| ENST00000585203.6:n.796+13G>A | ||
| NM_000018.3:c.1605+13G>A | NP_000009.1:n.1605+13G>A | |
| NM_001033859.2:c.1539+13G>A | NP_001029031.1:n.1539+13G>A | |
| NM_001270447.1:c.1674+13G>A | NP_001257376.1:n.1674+13G>A | |
| NM_001270448.1:c.1377+13G>A | NP_001257377.1:n.1377+13G>A | |
| XM_006721516.2:c.1605+13G>A | XP_006721579.2:n.1605+13G>A | |
| XM_011523829.1:c.1507+13G>A | XP_011522131.1:n.1507+13G>A | |
| XM_011523830.1:c.1507+13G>A | XP_011522132.1:n.1507+13G>A | |
| XR_934021.1:n.1712+13G>A | ||
| XR_934022.1:n.1614+13G>A | ||
| XR_934023.1:n.1614+13G>A | ||
| XM_006721516.3:c.1605+13G>A | XP_006721579.2:n.1605+13G>A | |
| XM_011523829.2:c.1507+13G>A | XP_011522131.1:n.1507+13G>A | |
| XM_011523830.2:c.1507+13G>A | XP_011522132.1:n.1507+13G>A | |
| XM_024450741.1:c.1520G>A | XP_024306509.1:p.Gly507Glu | |
| XR_934021.2:n.1664+13G>A | ||
| XR_934022.2:n.1566+13G>A | ||
| XR_934023.2:n.1566+13G>A | ||
| NM_000018.4:c.1605+13G>A MANE Select | NP_000009.1:n.1605+13G>A | |
| NM_001033859.3:c.1539+13G>A | NP_001029031.1:n.1539+13G>A | |
| NM_001270447.2:c.1674+13G>A | NP_001257376.1:n.1674+13G>A | |
| NM_001270448.2:c.1377+13G>A | NP_001257377.1:n.1377+13G>A |