Linked Data
ClinVar Variation Id:
134120
dbSNP Id:
rs4150521
ExAC:
2:128016978 G / A
gnomAD v2:
2-128016978-G-A
gnomAD v3:
2-127259402-G-A
gnomAD v4:
2-127259402-G-A
PubMed:
PMID:24728327
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.127259402G>A , CM000664.2:g.127259402G>A | GRCh38 |
| NC_000002.11:g.128016978G>A , CM000664.1:g.128016978G>A | GRCh37 |
| NC_000002.10:g.127733448G>A | NCBI36 |
| NG_007454.1:g.39775C>T , LRG_462:g.39775C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000285398.7:c.2111C>T MANE Select | ENSP00000285398.2:p.Ser704Leu | |
| ENST00000644317.1:c.*1600C>T | ENSP00000494012.1:n.*1600C>T | |
| ENST00000645233.1:c.*2323C>T | ENSP00000494116.1:n.*2323C>T | |
| ENST00000645467.1:c.*883C>T | ENSP00000494889.1:n.*883C>T | |
| ENST00000645736.1:c.1782C>T | ENSP00000494545.1:n.1782C>T | |
| ENST00000646042.1:n.2846C>T | ||
| ENST00000646654.1:c.*1578C>T | ENSP00000494526.1:n.*1578C>T | |
| ENST00000647169.1:c.2186C>T | ENSP00000495619.1:p.Ser729Leu | |
| ENST00000647496.1:c.396-1800C>T | ||
| ENST00000285398.6:c.2111C>T | ENSP00000285398.2:p.Ser704Leu | |
| ENST00000426778.5:c.*2092C>T | ENSP00000415335.1:n.*2092C>T | |
| ENST00000445889.5:c.*2154C>T | ENSP00000390888.1:n.*2154C>T | |
| ENST00000491292.5:n.3481C>T | ||
| NM_000122.1:c.2111C>T , LRG_462t1:c.2111C>T | NP_000113.1:p.Ser704Leu | |
| NM_001303416.1:c.1919C>T | NP_001290345.1:p.Ser640Leu | |
| NM_001303418.1:c.1919C>T | NP_001290347.1:p.Ser640Leu | |
| XM_011510794.1:c.2129C>T | XP_011509096.1:p.Ser710Leu | |
| XM_011510795.1:c.1673C>T | XP_011509097.1:p.Ser558Leu | |
| XM_011510794.2:c.2129C>T | XP_011509096.1:p.Ser710Leu | |
| XM_017003583.1:c.1655C>T | XP_016859072.1:p.Ser552Leu | |
| NM_000122.2:c.2111C>T MANE Select | NP_000113.1:p.Ser704Leu | |
| NM_001303416.2:c.1919C>T | NP_001290345.1:p.Ser640Leu | |
| NM_001303418.2:c.1919C>T | NP_001290347.1:p.Ser640Leu |