Linked Data
ClinVar Variation Id:
1042971
ClinVar RCV Id:
RCV001347010
dbSNP Id:
rs1039517619
gnomAD v3:
3-10142888-G-T
gnomAD v4:
3-10142888-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10142888G>T , CM000665.2:g.10142888G>T | GRCh38 |
| NC_000003.11:g.10184572G>T , CM000665.1:g.10184572G>T | GRCh37 |
| NC_000003.10:g.10159572G>T | NCBI36 |
| NG_008212.3:g.6254G>T , LRG_322:g.6254G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696142.1:c.466G>T | ENSP00000512434.1:p.Asp156Tyr | |
| ENST00000696143.1:c.466G>T | ENSP00000512435.1:p.Asp156Tyr | |
| ENST00000696153.1:c.340+701G>T | ENSP00000512444.1:n.340+701G>T | |
| ENST00000256474.3:c.340+701G>T MANE Select | ENSP00000256474.3:n.340+701G>T | |
| ENST00000256474.2:c.340+701G>T | ENSP00000256474.2:n.340+701G>T | |
| ENST00000345392.2:c.340+701G>T | ENSP00000344757.2:n.340+701G>T | |
| ENST00000477538.1:n.343G>T | ||
| NM_000551.3:c.340+701G>T , LRG_322t1:c.340+701G>T | NP_000542.1:n.340+701G>T | |
| NM_198156.2:c.340+701G>T | NP_937799.1:n.340+701G>T | |
| XM_011534078.1:c.466G>T | XP_011532380.1:p.Asp156Tyr | |
| NM_001354723.1:c.466G>T | NP_001341652.1:p.Asp156Tyr | |
| NM_000551.4:c.340+701G>T MANE Select | NP_000542.1:n.340+701G>T | |
| NM_001354723.2:c.466G>T | NP_001341652.1:p.Asp156Tyr | |
| NM_198156.3:c.340+701G>T | NP_937799.1:n.340+701G>T |