Linked Data
ClinVar Variation Id:
2164098
ClinVar RCV Id:
RCV003092673
dbSNP Id:
rs1190153122
gnomAD v2:
1-235969869-G-A
gnomAD v4:
1-235806569-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.235806569G>A , CM000663.2:g.235806569G>A | GRCh38 |
| NC_000001.10:g.235969869G>A , CM000663.1:g.235969869G>A | GRCh37 |
| NC_000001.9:g.234036492G>A | NCBI36 |
| NG_007397.1:g.82072C>T , LRG_143:g.82072C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000697178.1:c.2567C>T | ENSP00000513163.1:p.Thr856Ile | |
| ENST00000697242.1:c.1970C>T | ENSP00000513207.1:p.Thr657Ile | |
| ENST00000389793.7:c.2567C>T MANE Select | ENSP00000374443.2:p.Thr856Ile | |
| ENST00000389793.6:c.2567C>T | ENSP00000374443.2:p.Thr856Ile | |
| ENST00000389794.7:c.2567C>T | ENSP00000374444.4:p.Thr856Ile | |
| ENST00000465349.5:n.3118C>T | ||
| ENST00000489585.5:n.3118C>T | ||
| NM_000081.3:c.2567C>T , LRG_143t1:c.2567C>T | NP_000072.2:p.Thr856Ile | |
| NM_001301365.1:c.2567C>T , LRG_143t2:c.2567C>T | NP_001288294.1:p.Thr856Ile | |
| XM_011544031.1:c.2567C>T | XP_011542333.1:p.Thr856Ile | |
| XM_011544032.1:c.2567C>T | XP_011542334.1:p.Thr856Ile | |
| XM_011544033.1:c.2567C>T | XP_011542335.1:p.Thr856Ile | |
| XM_011544034.1:c.2567C>T | XP_011542336.1:p.Thr856Ile | |
| XM_011544035.1:c.2567C>T | XP_011542337.1:p.Thr856Ile | |
| XM_011544036.1:c.230C>T | XP_011542338.1:p.Thr77Ile | |
| XM_011544037.1:c.2567C>T | XP_011542339.1:p.Thr856Ile | |
| XM_011544038.1:c.2567C>T | XP_011542340.1:p.Thr856Ile | |
| XM_011544039.1:c.2567C>T | XP_011542341.1:p.Thr856Ile | |
| XM_011544040.1:c.2567C>T | XP_011542342.1:p.Thr856Ile | |
| XM_011544033.2:c.2567C>T | XP_011542335.1:p.Thr856Ile | |
| XM_011544035.2:c.2567C>T | XP_011542337.1:p.Thr856Ile | |
| XM_011544036.2:c.230C>T | XP_011542338.1:p.Thr77Ile | |
| XM_011544037.2:c.2567C>T | XP_011542339.1:p.Thr856Ile | |
| XM_011544039.2:c.2567C>T | XP_011542341.1:p.Thr856Ile | |
| XM_017000150.1:c.2567C>T | XP_016855639.1:p.Thr856Ile | |
| XM_017000151.1:c.2567C>T | XP_016855640.1:p.Thr856Ile | |
| XR_001736946.2:n.2749C>T | ||
| XR_001736947.1:n.2749C>T | ||
| XR_001736948.1:n.2749C>T | ||
| XR_002959252.1:n.2749C>T | ||
| NM_000081.4:c.2567C>T MANE Select | NP_000072.2:p.Thr856Ile |