Linked Data
ClinVar Variation Id:
1631373
dbSNP Id:
rs1391140770
gnomAD v2:
1-241667379-G-T
gnomAD v3:
1-241504079-G-T
gnomAD v4:
1-241504079-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.241504079G>T , CM000663.2:g.241504079G>T | GRCh38 |
| NC_000001.10:g.241667379G>T , CM000663.1:g.241667379G>T | GRCh37 |
| NC_000001.9:g.239734002G>T | NCBI36 |
| NG_012338.1:g.20676C>A , LRG_504:g.20676C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000493477.2:n.1574C>A | ||
| ENST00000682162.1:c.1100C>A | ENSP00000508203.1:n.1100C>A | |
| ENST00000682567.1:n.1148C>A | ||
| ENST00000683521.1:c.1071C>A | ENSP00000506864.1:p.Ile357= | |
| ENST00000684161.1:n.2286C>A | ||
| ENST00000684483.1:c.*467C>A | ENSP00000507894.1:n.*467C>A | |
| ENST00000366560.4:c.1071C>A MANE Select | ENSP00000355518.4:p.Ile357= | |
| ENST00000366560.3:c.1071C>A | ENSP00000355518.3:p.Ile357= | |
| NM_000143.3:c.1071C>A , LRG_504t1:c.1071C>A | NP_000134.2:p.Ile357= | |
| XM_011544132.1:c.843C>A | XP_011542434.1:p.Ile281= | |
| XM_011544132.2:c.843C>A | XP_011542434.1:p.Ile281= | |
| NM_000143.4:c.1071C>A MANE Select | NP_000134.2:p.Ile357= |