Linked Data
ClinVar Variation Id:
476884
dbSNP Id:
rs887057321
gnomAD v3:
5-149028301-C-T
gnomAD v4:
5-149028301-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149028301C>T , CM000667.2:g.149028301C>T | GRCh38 |
| NC_000005.9:g.148407864C>T , CM000667.1:g.148407864C>T | GRCh37 |
| NC_000005.8:g.148388057C>T | NCBI36 |
| NG_007947.2:g.39874G>A , LRG_269:g.39874G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502274.2:c.1395+56G>A | ||
| ENST00000515425.6:c.1431G>A MANE Select | ENSP00000423660.1:p.Glu477= | |
| ENST00000675793.1:c.*715G>A | ENSP00000502039.1:n.*715G>A | |
| ENST00000676056.1:c.*941G>A | ENSP00000501827.1:n.*941G>A | |
| ENST00000323829.9:c.*819G>A | ENSP00000313025.5:n.*819G>A | |
| ENST00000504517.5:c.961G>A | ENSP00000421779.1:n.961G>A | |
| ENST00000504690.5:c.1431G>A | ENSP00000425627.1:p.Glu477= | |
| ENST00000510779.1:c.481G>A | ||
| ENST00000511307.5:c.*1211G>A | ENSP00000421420.1:n.*1211G>A | |
| ENST00000512049.5:c.1410G>A | ENSP00000421860.1:p.Glu470= | |
| ENST00000513604.5:c.*819G>A | ENSP00000423111.1:n.*819G>A | |
| ENST00000515425.5:c.1431G>A | ENSP00000423660.1:p.Glu477= | |
| NM_024577.3:c.1431G>A , LRG_269t1:c.1431G>A | NP_078853.2:p.Glu477= | |
| NM_024577.4:c.1431G>A MANE Select | NP_078853.2:p.Glu477= |