Linked Data
ClinVar Variation Id:
36926
dbSNP Id:
rs387907246
ExAC:
7:66103899 C / T
gnomAD v2:
7-66103899-C-T
gnomAD v3:
7-66638912-C-T
gnomAD v4:
7-66638912-C-T
COSMIC:
COSM4618717
PubMed:
PMID:22748208
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.66638912C>T , CM000669.2:g.66638912C>T | GRCh38 |
| NC_000007.13:g.66103899C>T , CM000669.1:g.66103899C>T | GRCh37 |
| NC_000007.12:g.65741334C>T | NCBI36 |
| NG_028110.1:g.15032C>T | |
| NG_028110.2:g.15032C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000275532.8:c.510C>T | ENSP00000275532.4:p.Pro170= | |
| ENST00000449064.6:c.488C>T | ||
| ENST00000503687.2:c.380C>T | ENSP00000421074.1:p.Pro127Leu | |
| ENST00000638524.1:c.375C>T | ||
| ENST00000638540.1:c.354C>T | ||
| ENST00000639828.2:c.550C>T MANE Select | ENSP00000492240.1:p.Arg184Cys | |
| ENST00000639879.1:c.*413C>T | ENSP00000492161.1:n.*413C>T | |
| ENST00000640234.1:c.420C>T | ||
| ENST00000640385.1:c.550C>T | ENSP00000491193.1:p.Arg184Cys | |
| ENST00000640601.1:c.57C>T | ||
| ENST00000640851.1:c.550C>T | ENSP00000492577.1:p.Arg184Cys | |
| ENST00000275532.7:c.550C>T | ENSP00000275532.3:p.Arg184Cys | |
| ENST00000443322.1:c.550C>T | ENSP00000411624.1:p.Arg184Cys | |
| ENST00000449064.5:c.380C>T | ENSP00000388463.1:p.Pro127Leu | |
| ENST00000503687.1:c.380C>T | ENSP00000421074.1:p.Pro127Leu | |
| NM_001167961.2:c.550C>T | NP_001161433.1:p.Arg184Cys | |
| NM_153033.4:c.550C>T | NP_694578.1:p.Arg184Cys | |
| NM_153033.5:c.550C>T MANE Select | NP_694578.1:p.Arg184Cys |