Linked Data
dbSNP Id:
rs768365263
ExAC:
3:133494275 A / G
gnomAD v2:
3-133494275-A-G
gnomAD v4:
3-133775431-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.133775431A>G , CM000665.2:g.133775431A>G | GRCh38 |
| NC_000003.11:g.133494275A>G , CM000665.1:g.133494275A>G | GRCh37 |
| NC_000003.10:g.134976965A>G | NCBI36 |
| NG_013080.1:g.34299A>G | |
| NG_013080.2:g.118434A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000402696.9:c.1688-2A>G MANE Select | ENSP00000385834.3:n.1688-2A>G | |
| ENST00000402696.7:c.1688-2A>G | ENSP00000385834.3:n.1688-2A>G | |
| ENST00000461695.1:c.419-2A>G | ||
| ENST00000467842.1:n.2680A>G | ||
| NM_001063.3:c.1688-2A>G | NP_001054.1:n.1688-2A>G | |
| XM_011513100.1:c.1688-2A>G | XP_011511402.1:n.1688-2A>G | |
| NM_001354703.1:c.1556-2A>G | NP_001341632.1:n.1556-2A>G | |
| NM_001354704.1:c.1307-2A>G | NP_001341633.1:n.1307-2A>G | |
| NM_001063.4:c.1688-2A>G MANE Select | NP_001054.2:n.1688-2A>G | |
| NM_001354703.2:c.1556-2A>G | NP_001341632.2:n.1556-2A>G | |
| NM_001354704.2:c.1307-2A>G | NP_001341633.2:n.1307-2A>G |