Linked Data
dbSNP Id:
rs1623879
gnomAD v2:
3-58027197-A-G
gnomAD v3:
3-58041470-A-G
gnomAD v4:
3-58041470-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.58041470A>G , CM000665.2:g.58041470A>G | GRCh38 |
| NC_000003.11:g.58027197A>G , CM000665.1:g.58027197A>G | GRCh37 |
| NC_000003.10:g.58002237A>G | NCBI36 |
| NG_012801.1:g.38071A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000682097.1:c.292+32614A>G | ENSP00000508183.1:n.292+32614A>G | |
| ENST00000682868.1:n.435+32614A>G | ||
| ENST00000682871.1:c.292+32614A>G | ENSP00000507805.1:n.292+32614A>G | |
| ENST00000682987.1:n.435+32614A>G | ||
| ENST00000683511.1:n.451+32614A>G | ||
| ENST00000684107.1:c.292+32614A>G | ENSP00000507440.1:n.292+32614A>G | |
| ENST00000684506.1:c.292+32614A>G | ENSP00000507728.1:n.292+32614A>G | |
| ENST00000684517.1:c.292+32614A>G | ENSP00000507828.1:n.292+32614A>G | |
| ENST00000684607.1:c.292+32614A>G | ENSP00000508224.1:n.292+32614A>G | |
| ENST00000295956.9:c.292+32614A>G MANE Select | ENSP00000295956.5:n.292+32614A>G | |
| ENST00000295956.8:c.292+32614A>G | ENSP00000295956.4:n.292+32614A>G | |
| ENST00000358537.7:c.292+32614A>G | ENSP00000351339.3:n.292+32614A>G | |
| ENST00000429972.6:c.292+32614A>G | ENSP00000415599.2:n.292+32614A>G | |
| ENST00000490882.5:c.292+32614A>G | ENSP00000420213.1:n.292+32614A>G | |
| NM_001164317.1:c.292+32614A>G | NP_001157789.1:n.292+32614A>G | |
| NM_001164318.1:c.292+32614A>G | NP_001157790.1:n.292+32614A>G | |
| NM_001164319.1:c.292+32614A>G | NP_001157791.1:n.292+32614A>G | |
| NM_001457.3:c.292+32614A>G | NP_001448.2:n.292+32614A>G | |
| XM_005264977.1:c.292+32614A>G | XP_005265034.1:n.292+32614A>G | |
| XM_005264978.1:c.292+32614A>G | XP_005265035.1:n.292+32614A>G | |
| XM_005264981.1:c.292+32614A>G | XP_005265038.1:n.292+32614A>G | |
| XR_940396.1:n.437+32614A>G | ||
| XM_005264978.2:c.292+32614A>G | XP_005265035.1:n.292+32614A>G | |
| XR_001740065.1:n.437+32614A>G | ||
| XR_940396.2:n.437+32614A>G | ||
| NM_001164317.2:c.292+32614A>G | NP_001157789.1:n.292+32614A>G | |
| NM_001164318.2:c.292+32614A>G | NP_001157790.1:n.292+32614A>G | |
| NM_001164319.2:c.292+32614A>G | NP_001157791.1:n.292+32614A>G | |
| NM_001457.4:c.292+32614A>G MANE Select | NP_001448.2:n.292+32614A>G |