Linked Data
ClinVar Variation Id:
1142914
ClinVar RCV Id:
RCV001480861
dbSNP Id:
rs1238822178
gnomAD v2:
5-148406281-G-A
gnomAD v4:
5-149026718-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149026718G>A , CM000667.2:g.149026718G>A | GRCh38 |
| NC_000005.9:g.148406281G>A , CM000667.1:g.148406281G>A | GRCh37 |
| NC_000005.8:g.148386474G>A | NCBI36 |
| NG_007947.2:g.41457C>T , LRG_269:g.41457C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502274.2:c.2803C>T | ||
| ENST00000515425.6:c.2907C>T MANE Select | ENSP00000423660.1:p.Phe969= | |
| ENST00000675793.1:c.*2191C>T | ENSP00000502039.1:n.*2191C>T | |
| ENST00000676056.1:c.*2417C>T | ENSP00000501827.1:n.*2417C>T | |
| ENST00000323829.9:c.*2295C>T | ENSP00000313025.5:n.*2295C>T | |
| ENST00000504517.5:c.2437C>T | ENSP00000421779.1:n.2437C>T | |
| ENST00000504690.5:c.2907C>T | ENSP00000425627.1:p.Phe969= | |
| ENST00000510779.1:c.1957C>T | ||
| ENST00000511307.5:c.*2794C>T | ENSP00000421420.1:n.*2794C>T | |
| ENST00000512049.5:c.2886C>T | ENSP00000421860.1:p.Phe962= | |
| ENST00000513604.5:c.*2402C>T | ENSP00000423111.1:n.*2402C>T | |
| ENST00000515425.5:c.2907C>T | ENSP00000423660.1:p.Phe969= | |
| NM_024577.3:c.2907C>T , LRG_269t1:c.2907C>T | NP_078853.2:p.Phe969= | |
| NM_024577.4:c.2907C>T MANE Select | NP_078853.2:p.Phe969= |