Linked Data
dbSNP Id:
rs1298946357
gnomAD v2:
3-45518276-A-G
gnomAD v3:
3-45476784-A-G
gnomAD v4:
3-45476784-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.45476784A>G , CM000665.2:g.45476784A>G | GRCh38 |
| NC_000003.11:g.45518276A>G , CM000665.1:g.45518276A>G | GRCh37 |
| NC_000003.10:g.45493280A>G | NCBI36 |
| NG_033907.1:g.93202A>G | |
| NG_033907.2:g.93202A>G | |
| NG_033907.3:g.93221A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265537.8:c.1018+157A>G | ENSP00000265537.4:n.1018+157A>G | |
| ENST00000642274.1:c.1018+157A>G | ENSP00000495707.1:n.1018+157A>G | |
| ENST00000645846.2:c.1018+157A>G MANE Select | ENSP00000495093.1:n.1018+157A>G | |
| ENST00000650792.2:c.1018+157A>G | ENSP00000498867.1:n.1018+157A>G | |
| ENST00000651549.1:c.1018+157A>G | ENSP00000499002.1:n.1018+157A>G | |
| ENST00000652135.1:c.*886+157A>G | ENSP00000499104.1:n.*886+157A>G | |
| ENST00000265537.7:c.1018+157A>G | ENSP00000265537.3:n.1018+157A>G | |
| ENST00000414984.5:c.889+157A>G | ENSP00000412893.1:n.889+157A>G | |
| ENST00000415258.5:c.1018+157A>G | ENSP00000408576.1:n.1018+157A>G | |
| NM_015340.3:c.1018+157A>G | NP_056155.1:n.1018+157A>G | |
| XM_005265006.1:c.1018+157A>G | XP_005265063.1:n.1018+157A>G | |
| XM_011533554.1:c.1018+157A>G | XP_011531856.1:n.1018+157A>G | |
| XM_005265006.2:c.1018+157A>G | XP_005265063.1:n.1018+157A>G | |
| XM_011533554.2:c.1018+157A>G | XP_011531856.1:n.1018+157A>G | |
| XM_017006042.1:c.1018+157A>G | XP_016861531.1:n.1018+157A>G | |
| NM_015340.4:c.1018+157A>G MANE Select | NP_056155.1:n.1018+157A>G | |
| NM_001368263.1:c.1018+157A>G | NP_001355192.1:n.1018+157A>G |