Linked Data
ClinVar Variation Id:
1611730
ClinVar RCV Id:
RCV002166069
dbSNP Id:
rs201013419
gnomAD v4:
3-122257171-G-T
MyVariant Identifiers:
chr3:g.121976018G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.122257171G>T , CM000665.2:g.122257171G>T | GRCh38 |
| NC_000003.11:g.121976018G>T , CM000665.1:g.121976018G>T | GRCh37 |
| NC_000003.10:g.123458708G>T | NCBI36 |
| NG_009058.1:g.78489G>T | |
| NG_009058.2:g.78504G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000490131.7:c.276G>T | ENSP00000418685.2:p.Thr92= | |
| ENST00000498619.4:c.276G>T | ENSP00000420194.1:p.Thr92= | |
| ENST00000638296.1:n.195G>T | ||
| ENST00000638421.1:c.276G>T | ENSP00000492190.1:p.Thr92= | |
| ENST00000639785.2:c.276G>T MANE Select | ENSP00000491584.2:p.Thr92= | |
| ENST00000490131.5:c.276G>T | ENSP00000418685.1:p.Thr92= | |
| ENST00000490186.1:n.135G>T | ||
| ENST00000498619.2:c.276G>T | ENSP00000420194.1:p.Thr92= | |
| NM_000388.3:c.276G>T | NP_000379.2:p.Thr92= | |
| NM_001178065.1:c.276G>T | NP_001171536.1:p.Thr92= | |
| XM_005247836.2:c.276G>T | XP_005247893.1:p.Thr92= | |
| XM_005247837.2:c.9+2797G>T | XP_005247894.1:n.9+2797G>T | |
| XM_006713789.2:c.276G>T | XP_006713852.1:p.Thr92= | |
| XM_011513237.1:c.276G>T | XP_011511539.1:p.Thr92= | |
| XM_011513238.1:c.276G>T | XP_011511540.1:p.Thr92= | |
| XM_006713789.3:c.276G>T | XP_006713852.1:p.Thr92= | |
| XM_017007324.1:c.276G>T | XP_016862813.1:p.Thr92= | |
| XM_017007325.1:c.276G>T | XP_016862814.1:p.Thr92= | |
| NM_000388.4:c.276G>T MANE Select | NP_000379.3:p.Thr92= | |
| NM_001178065.2:c.276G>T | NP_001171536.2:p.Thr92= |