Linked Data
ClinVar Variation Id:
2935227
ClinVar RCV Id:
RCV003790881
dbSNP Id:
rs1402764615
gnomAD v2:
1-6534533-C-T
gnomAD v3:
1-6474473-C-T
gnomAD v4:
1-6474473-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.6474473C>T , CM000663.2:g.6474473C>T | GRCh38 |
| NC_000001.10:g.6534533C>T , CM000663.1:g.6534533C>T | GRCh37 |
| NC_000001.9:g.6457120C>T | NCBI36 |
| NG_007978.1:g.50537G>A , LRG_262:g.50537G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340850.10:c.417G>A | ENSP00000344570.5:p.Gly139= | |
| ENST00000377728.8:c.417G>A MANE Select | ENSP00000366957.3:p.Gly139= | |
| ENST00000377740.5:c.417G>A | ENSP00000366969.4:p.Gly139= | |
| ENST00000377748.6:c.591G>A | ENSP00000366977.2:p.Gly197= | |
| ENST00000400913.6:c.417G>A | ENSP00000383704.1:p.Gly139= | |
| ENST00000400915.8:c.528G>A | ENSP00000383706.4:p.Gly176= | |
| ENST00000489097.6:n.893G>A | ||
| ENST00000535355.6:c.624G>A | ENSP00000441445.1:p.Gly208= | |
| ENST00000537245.6:c.528G>A | ENSP00000439625.2:p.Gly176= | |
| ENST00000673471.2:c.714G>A | ENSP00000500749.1:p.Gly238= | |
| ENST00000674790.1:c.*629G>A | ENSP00000502815.1:n.*629G>A | |
| ENST00000675123.1:c.417G>A | ENSP00000502132.1:p.Gly139= | |
| ENST00000675548.1:c.*245G>A | ENSP00000502684.1:n.*245G>A | |
| ENST00000675694.1:c.417G>A | ENSP00000501925.1:p.Gly139= | |
| ENST00000676255.1:c.379G>A | ENSP00000502459.1:n.379G>A | |
| ENST00000340850.9:c.417G>A | ENSP00000344570.5:p.Gly139= | |
| ENST00000377725.5:c.417G>A | ENSP00000366954.1:p.Gly139= | |
| ENST00000377728.7:c.417G>A | ENSP00000366957.3:p.Gly139= | |
| ENST00000377732.5:c.528G>A | ENSP00000366961.1:p.Gly176= | |
| ENST00000377740.4:c.648G>A | ENSP00000366969.3:p.Gly216= | |
| ENST00000377748.5:c.648G>A | ENSP00000366977.1:p.Gly216= | |
| ENST00000400913.5:c.417G>A | ENSP00000383704.1:p.Gly139= | |
| ENST00000400915.7:c.585G>A | ENSP00000383706.3:p.Gly195= | |
| ENST00000489097.5:n.893G>A | ||
| ENST00000535355.5:c.624G>A | ENSP00000441445.1:p.Gly208= | |
| ENST00000537245.5:c.654G>A | ENSP00000439625.1:p.Gly218= | |
| NM_001042663.1:c.585G>A | NP_001036128.1:p.Gly195= | |
| NM_001042664.1:c.417G>A | NP_001036129.1:p.Gly139= | |
| NM_001042665.1:c.417G>A | NP_001036130.1:p.Gly139= | |
| NM_001265592.1:c.654G>A | NP_001252521.1:p.Gly218= | |
| NM_001265593.1:c.624G>A | NP_001252522.1:p.Gly208= | |
| NM_001265594.1:c.417G>A | NP_001252523.1:p.Gly139= | |
| NM_020631.4:c.417G>A | NP_065682.2:p.Gly139= | |
| NM_198681.3:c.648G>A | NP_941374.2:p.Gly216= | |
| NM_001042663.2:c.585G>A | NP_001036128.1:p.Gly195= | |
| NM_001265594.2:c.417G>A | NP_001252523.1:p.Gly139= | |
| NM_020631.5:c.417G>A | NP_065682.2:p.Gly139= | |
| NM_001042663.3:c.528G>A | NP_001036128.2:p.Gly176= | |
| NM_001265592.2:c.528G>A | NP_001252521.2:p.Gly176= | |
| NM_020631.6:c.417G>A MANE Select | NP_065682.2:p.Gly139= | |
| NM_198681.4:c.417G>A | NP_941374.3:p.Gly139= |