Linked Data
ClinVar Variation Id:
297933
dbSNP Id:
rs886046497
gnomAD v3:
1-6467884-G-A
gnomAD v4:
1-6467884-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.6467884G>A , CM000663.2:g.6467884G>A | GRCh38 |
| NC_000001.10:g.6527944G>A , CM000663.1:g.6527944G>A | GRCh37 |
| NC_000001.9:g.6450531G>A | NCBI36 |
| NG_007978.1:g.57126C>T , LRG_262:g.57126C>T | |
| NG_029910.1:g.3312C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340850.10:c.2952C>T | ENSP00000344570.5:p.Thr984= | |
| ENST00000377728.8:c.2952C>T MANE Select | ENSP00000366957.3:p.Thr984= | |
| ENST00000377740.5:c.2952C>T | ENSP00000366969.4:p.Thr984= | |
| ENST00000377748.6:c.3126C>T | ENSP00000366977.2:p.Thr1042= | |
| ENST00000400913.6:c.2952C>T | ENSP00000383704.1:p.Thr984= | |
| ENST00000400915.8:c.3063C>T | ENSP00000383706.4:p.Thr1021= | |
| ENST00000489097.6:n.3428C>T | ||
| ENST00000535355.6:c.3159C>T | ENSP00000441445.1:p.Thr1053= | |
| ENST00000537245.6:c.3063C>T | ENSP00000439625.2:p.Thr1021= | |
| ENST00000673471.2:c.3249C>T | ENSP00000500749.1:p.Thr1083= | |
| ENST00000674790.1:c.*3164C>T | ENSP00000502815.1:n.*3164C>T | |
| ENST00000675123.1:c.2259C>T | ENSP00000502132.1:p.Thr753= | |
| ENST00000675548.1:c.*2780C>T | ENSP00000502684.1:n.*2780C>T | |
| ENST00000675694.1:c.2952C>T | ENSP00000501925.1:p.Thr984= | |
| ENST00000675976.1:c.825C>T | ENSP00000501611.1:p.Thr275= | |
| ENST00000340850.9:c.2952C>T | ENSP00000344570.5:p.Thr984= | |
| ENST00000377725.5:c.2752C>T | ENSP00000366954.1:p.Pro918Ser | |
| ENST00000377728.7:c.2952C>T | ENSP00000366957.3:p.Thr984= | |
| ENST00000377732.5:c.3063C>T | ENSP00000366961.1:p.Thr1021= | |
| ENST00000377740.4:c.2490C>T | ENSP00000366969.3:p.Thr830= | |
| ENST00000377748.5:c.3183C>T | ENSP00000366977.1:p.Thr1061= | |
| ENST00000400913.5:c.2952C>T | ENSP00000383704.1:p.Thr984= | |
| ENST00000400915.7:c.3120C>T | ENSP00000383706.3:p.Thr1040= | |
| ENST00000487949.4:n.2154C>T | ||
| ENST00000489097.5:n.3428C>T | ||
| ENST00000535355.5:c.3159C>T | ENSP00000441445.1:p.Thr1053= | |
| ENST00000537245.5:c.3189C>T | ENSP00000439625.1:p.Thr1063= | |
| NM_001042663.1:c.3120C>T | NP_001036128.1:p.Thr1040= | |
| NM_001042664.1:c.2952C>T | NP_001036129.1:p.Thr984= | |
| NM_001042665.1:c.2952C>T | NP_001036130.1:p.Thr984= | |
| NM_001265592.1:c.3189C>T | NP_001252521.1:p.Thr1063= | |
| NM_001265593.1:c.3159C>T | NP_001252522.1:p.Thr1053= | |
| NM_001265594.1:c.2752C>T | NP_001252523.1:p.Pro918Ser | |
| NM_020631.4:c.2952C>T | NP_065682.2:p.Thr984= | |
| NM_198681.3:c.3183C>T | NP_941374.2:p.Thr1061= | |
| NM_001042663.2:c.3120C>T | NP_001036128.1:p.Thr1040= | |
| NM_001265594.2:c.2752C>T | NP_001252523.1:p.Pro918Ser | |
| NM_020631.5:c.2952C>T | NP_065682.2:p.Thr984= | |
| NM_001042663.3:c.3063C>T | NP_001036128.2:p.Thr1021= | |
| NM_001265592.2:c.3063C>T | NP_001252521.2:p.Thr1021= | |
| NM_020631.6:c.2952C>T MANE Select | NP_065682.2:p.Thr984= | |
| NM_198681.4:c.2952C>T | NP_941374.3:p.Thr984= |