Linked Data
ClinVar Variation Id:
237110
dbSNP Id:
rs201115573
ExAC:
1:241661199 C / T
gnomAD v2:
1-241661199-C-T
gnomAD v3:
1-241497899-C-T
gnomAD v4:
1-241497899-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.241497899C>T , CM000663.2:g.241497899C>T | GRCh38 |
| NC_000001.10:g.241661199C>T , CM000663.1:g.241661199C>T | GRCh37 |
| NC_000001.9:g.239727822C>T | NCBI36 |
| NG_012338.1:g.26856G>A , LRG_504:g.26856G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000493477.2:n.1965G>A | ||
| ENST00000682162.1:c.1491G>A | ENSP00000508203.1:n.1491G>A | |
| ENST00000682567.1:n.4862G>A | ||
| ENST00000684161.1:n.2677G>A | ||
| ENST00000684483.1:c.*858G>A | ENSP00000507894.1:n.*858G>A | |
| ENST00000366560.4:c.1462G>A MANE Select | ENSP00000355518.4:p.Glu488Lys | |
| ENST00000366560.3:c.1462G>A | ENSP00000355518.3:p.Glu488Lys | |
| NM_000143.3:c.1462G>A , LRG_504t1:c.1462G>A | NP_000134.2:p.Glu488Lys | |
| XM_011544132.1:c.1234G>A | XP_011542434.1:p.Glu412Lys | |
| XM_011544132.2:c.1234G>A | XP_011542434.1:p.Glu412Lys | |
| NM_000143.4:c.1462G>A MANE Select | NP_000134.2:p.Glu488Lys |