Linked Data
dbSNP Id:
rs145625338
ExAC:
6:129802621 A / G
gnomAD v2:
6-129802621-A-G
gnomAD v3:
6-129481476-A-G
gnomAD v4:
6-129481476-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.129481476A>G , CM000668.2:g.129481476A>G | GRCh38 |
| NC_000006.11:g.129802621A>G , CM000668.1:g.129802621A>G | GRCh37 |
| NC_000006.10:g.129844314A>G | NCBI36 |
| NG_008678.1:g.603336A>G , LRG_409:g.603336A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000617695.5:c.7737+37A>G | ENSP00000481744.2:n.7737+37A>G | |
| ENST00000618192.5:c.8013+37A>G | ENSP00000480802.2:n.8013+37A>G | |
| ENST00000421865.3:c.7749+37A>G MANE Select | ENSP00000400365.2:n.7749+37A>G | |
| ENST00000421865.2:c.7749+37A>G | ENSP00000400365.2:n.7749+37A>G | |
| ENST00000617695.4:c.7737+37A>G | ENSP00000481744.1:n.7737+37A>G | |
| ENST00000618192.4:c.7746+37A>G | ENSP00000480802.1:n.7746+37A>G | |
| NM_000426.3:c.7749+37A>G , LRG_409t1:c.7749+37A>G | NP_000417.2:n.7749+37A>G | |
| NM_001079823.1:c.7737+37A>G | NP_001073291.1:n.7737+37A>G | |
| XM_005266981.2:c.8013+37A>G | XP_005267038.1:n.8013+37A>G | |
| XM_005266982.2:c.8001+37A>G | XP_005267039.1:n.8001+37A>G | |
| XM_011535820.1:c.8007+37A>G | XP_011534122.1:n.8007+37A>G | |
| XM_005266981.3:c.8013+37A>G | XP_005267038.1:n.8013+37A>G | |
| XM_005266982.3:c.8001+37A>G | XP_005267039.1:n.8001+37A>G | |
| XM_011535820.2:c.8007+37A>G | XP_011534122.1:n.8007+37A>G | |
| XM_017010851.2:c.8019+37A>G | XP_016866340.1:n.8019+37A>G | |
| XM_017010852.1:c.6144+37A>G | XP_016866341.1:n.6144+37A>G | |
| NM_000426.4:c.7749+37A>G MANE Select | NP_000417.3:n.7749+37A>G | |
| NM_001079823.2:c.7737+37A>G | NP_001073291.2:n.7737+37A>G |