Linked Data
ClinVar Variation Id:
405931
dbSNP Id:
rs370392829
ExAC:
1:241680542 G / A
gnomAD v2:
1-241680542-G-A
gnomAD v3:
1-241517242-G-A
gnomAD v4:
1-241517242-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.241517242G>A , CM000663.2:g.241517242G>A | GRCh38 |
| NC_000001.10:g.241680542G>A , CM000663.1:g.241680542G>A | GRCh37 |
| NC_000001.9:g.239747165G>A | NCBI36 |
| NG_012338.1:g.7513C>T , LRG_504:g.7513C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000493477.2:n.710C>T | ||
| ENST00000682162.1:c.236C>T | ENSP00000508203.1:n.236C>T | |
| ENST00000682567.1:n.284C>T | ||
| ENST00000683521.1:c.207C>T | ENSP00000506864.1:p.Gly69= | |
| ENST00000684483.1:c.207C>T | ENSP00000507894.1:p.Gly69= | |
| ENST00000366560.4:c.207C>T MANE Select | ENSP00000355518.4:p.Gly69= | |
| ENST00000366560.3:c.207C>T | ENSP00000355518.3:p.Gly69= | |
| ENST00000493477.1:n.320C>T | ||
| NM_000143.3:c.207C>T , LRG_504t1:c.207C>T | NP_000134.2:p.Gly69= | |
| XM_011544132.1:c.-22C>T | XP_011542434.1:n.-22C>T | |
| XM_011544132.2:c.-22C>T | XP_011542434.1:n.-22C>T | |
| NM_000143.4:c.207C>T MANE Select | NP_000134.2:p.Gly69= |