Linked Data
ClinVar Variation Id:
205374
dbSNP Id:
rs144915847
ExAC:
20:62562301 C / T
gnomAD v2:
20-62562301-C-T
gnomAD v3:
20-63930948-C-T
gnomAD v4:
20-63930948-C-T
COSMIC:
COSM382871
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.63930948C>T , CM000682.2:g.63930948C>T | GRCh38 |
| NC_000020.10:g.62562301C>T , CM000682.1:g.62562301C>T | GRCh37 |
| NC_000020.9:g.62032745C>T | NCBI36 |
| NG_029805.1:g.40847C>T | |
| NG_029805.2:g.40847C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703637.1:c.419C>T | ENSP00000515413.1:p.Ala140Val | |
| ENST00000360864.9:c.419C>T MANE Select | ENSP00000354111.4:p.Ala140Val | |
| ENST00000360864.8:c.419C>T | ENSP00000354111.4:p.Ala140Val | |
| ENST00000470551.1:c.419C>T | ENSP00000434744.1:p.Ala140Val | |
| NM_025219.2:c.419C>T | NP_079495.1:p.Ala140Val | |
| XM_011529048.1:c.419C>T | XP_011527350.1:p.Ala140Val | |
| XM_011529049.1:c.419C>T | XP_011527351.1:p.Ala140Val | |
| XM_011529050.1:c.419C>T | XP_011527352.1:p.Ala140Val | |
| XR_936629.1:n.1051C>T | ||
| XR_936630.1:n.1309C>T | ||
| XM_011529048.2:c.419C>T | XP_011527350.1:p.Ala140Val | |
| XR_936629.2:n.1064C>T | ||
| NM_025219.3:c.419C>T MANE Select | NP_079495.1:p.Ala140Val |