Linked Data
ClinVar Variation Id:
448364
dbSNP Id:
rs138967360
ExAC:
5:148407969 C / T
gnomAD v2:
5-148407969-C-T
gnomAD v3:
5-149028406-C-T
gnomAD v4:
5-149028406-C-T
PubMed:
PMID:26785492
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149028406C>T , CM000667.2:g.149028406C>T | GRCh38 |
| NC_000005.9:g.148407969C>T , CM000667.1:g.148407969C>T | GRCh37 |
| NC_000005.8:g.148388162C>T | NCBI36 |
| NG_007947.2:g.39769G>A , LRG_269:g.39769G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502274.2:c.1346G>A | ||
| ENST00000515425.6:c.1326G>A MANE Select | ENSP00000423660.1:p.Pro442= | |
| ENST00000675793.1:c.*610G>A | ENSP00000502039.1:n.*610G>A | |
| ENST00000676056.1:c.*836G>A | ENSP00000501827.1:n.*836G>A | |
| ENST00000323829.9:c.*714G>A | ENSP00000313025.5:n.*714G>A | |
| ENST00000504517.5:c.856G>A | ENSP00000421779.1:n.856G>A | |
| ENST00000504690.5:c.1326G>A | ENSP00000425627.1:p.Pro442= | |
| ENST00000510779.1:c.376G>A | ||
| ENST00000511307.5:c.*1106G>A | ENSP00000421420.1:n.*1106G>A | |
| ENST00000512049.5:c.1305G>A | ENSP00000421860.1:p.Pro435= | |
| ENST00000513340.1:n.700G>A | ||
| ENST00000513604.5:c.*714G>A | ENSP00000423111.1:n.*714G>A | |
| ENST00000515425.5:c.1326G>A | ENSP00000423660.1:p.Pro442= | |
| NM_024577.3:c.1326G>A , LRG_269t1:c.1326G>A | NP_078853.2:p.Pro442= | |
| NM_024577.4:c.1326G>A MANE Select | NP_078853.2:p.Pro442= |