Linked Data
dbSNP Id:
rs1317647279
gnomAD v2:
1-983110-G-T
gnomAD v3:
1-1047730-G-T
gnomAD v4:
1-1047730-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.1047730G>T , CM000663.2:g.1047730G>T | GRCh38 |
| NC_000001.10:g.983110G>T , CM000663.1:g.983110G>T | GRCh37 |
| NC_000001.9:g.972973G>T | NCBI36 |
| NG_016346.1:g.32608G>T , LRG_198:g.32608G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379370.7:c.3631+43G>T MANE Select | ENSP00000368678.2:n.3631+43G>T | |
| ENST00000651234.1:c.3316+43G>T | ENSP00000499046.1:n.3316+43G>T | |
| ENST00000652369.1:c.3316+43G>T | ENSP00000498543.1:n.3316+43G>T | |
| ENST00000379370.6:c.3631+43G>T | ENSP00000368678.2:n.3631+43G>T | |
| ENST00000466223.1:n.369+43G>T | ||
| ENST00000478677.1:n.213+43G>T | ||
| ENST00000620552.4:c.3217+43G>T | ENSP00000484607.1:n.3217+43G>T | |
| NM_001305275.1:c.3631+43G>T | NP_001292204.1:n.3631+43G>T | |
| NM_198576.3:c.3631+43G>T | NP_940978.2:n.3631+43G>T | |
| XM_005244749.2:c.3631+43G>T | XP_005244806.1:n.3631+43G>T | |
| XM_006710635.2:c.3631+43G>T | XP_006710698.1:n.3631+43G>T | |
| XM_011541429.1:c.3631+43G>T | XP_011539731.1:n.3631+43G>T | |
| XM_011541430.1:c.2758+43G>T | XP_011539732.1:n.2758+43G>T | |
| XM_011541431.1:c.1897+43G>T | XP_011539733.1:n.1897+43G>T | |
| XR_946650.1:n.3698+43G>T | ||
| NM_001364727.1:c.3316+43G>T | NP_001351656.1:n.3316+43G>T | |
| XM_005244749.3:c.3631+43G>T | XP_005244806.1:n.3631+43G>T | |
| XM_011541429.2:c.3631+43G>T | XP_011539731.1:n.3631+43G>T | |
| XR_946650.2:n.3702+43G>T | ||
| NM_001305275.2:c.3631+43G>T | NP_001292204.1:n.3631+43G>T | |
| NM_198576.4:c.3631+43G>T MANE Select | NP_940978.2:n.3631+43G>T | |
| NM_001364727.2:c.3316+43G>T | NP_001351656.1:n.3316+43G>T |