Linked Data
ClinVar Variation Id:
21821
dbSNP Id:
rs61884288
ExAC:
11:18303533 G / A
gnomAD v2:
11-18303533-G-A
gnomAD v3:
11-18281986-G-A
gnomAD v4:
11-18281986-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.18281986G>A , CM000673.2:g.18281986G>A | GRCh38 |
| NC_000011.9:g.18303533G>A , CM000673.1:g.18303533G>A | GRCh37 |
| NC_000011.8:g.18260109G>A | NCBI36 |
| NG_008877.1:g.45189C>T , LRG_586:g.45189C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000349215.8:c.3293C>T MANE Select | ENSP00000265967.5:p.Thr1098Ile | |
| ENST00000349215.7:c.3293C>T | ENSP00000265967.5:p.Thr1098Ile | |
| ENST00000352460.7:n.1570C>T | ||
| ENST00000396253.7:c.2951C>T | ENSP00000379552.3:p.Thr984Ile | |
| ENST00000438420.6:c.2951C>T | ENSP00000399590.2:p.Thr984Ile | |
| ENST00000537258.1:c.614C>T | ENSP00000437437.1:p.Thr205Ile | |
| NM_007216.3:c.2951C>T | NP_009147.3:p.Thr984Ile | |
| NM_181507.1:c.3293C>T , LRG_586t1:c.3293C>T | NP_852608.1:p.Thr1098Ile | |
| NM_181508.1:c.2951C>T | NP_852609.1:p.Thr984Ile | |
| XM_011519862.1:c.3293C>T | XP_011518164.1:p.Thr1098Ile | |
| XM_011519863.1:c.3293C>T | XP_011518165.1:p.Thr1098Ile | |
| XM_011519864.1:c.3293C>T | XP_011518166.1:p.Thr1098Ile | |
| XM_011519865.1:c.3182C>T | XP_011518167.1:p.Thr1061Ile | |
| XM_011519866.1:c.2951C>T | XP_011518168.1:p.Thr984Ile | |
| XM_011519867.1:c.2951C>T | XP_011518169.1:p.Thr984Ile | |
| XM_011519868.1:c.2951C>T | XP_011518170.1:p.Thr984Ile | |
| XM_011519868.3:c.2951C>T | XP_011518170.1:p.Thr984Ile | |
| XM_017017149.1:c.3293C>T | XP_016872638.1:p.Thr1098Ile | |
| XM_017017150.1:c.3293C>T | XP_016872639.1:p.Thr1098Ile | |
| XM_017017151.2:c.3182C>T | XP_016872640.1:p.Thr1061Ile | |
| XM_017017152.1:c.3182C>T | XP_016872641.1:p.Thr1061Ile | |
| XM_017017153.2:c.3182C>T | XP_016872642.1:p.Thr1061Ile | |
| XM_017017154.1:c.2951C>T | XP_016872643.1:p.Thr984Ile | |
| XR_001747750.1:n.3455C>T | ||
| XR_001747751.1:n.3622C>T | ||
| XR_001747752.1:n.3211C>T | ||
| XR_001747753.1:n.3328C>T | ||
| XR_001747754.2:n.2959C>T | ||
| XR_001747755.2:n.2881C>T | ||
| XR_001747756.2:n.2954C>T | ||
| NM_007216.4:c.2951C>T | NP_009147.3:p.Thr984Ile | |
| NM_181507.2:c.3293C>T MANE Select | NP_852608.1:p.Thr1098Ile |