Linked Data
ClinVar Variation Id:
317991
ClinVar RCV Id:
RCV000325644
dbSNP Id:
rs776522454
ExAC:
16:1569896 G / A
gnomAD v2:
16-1569896-G-A
gnomAD v3:
16-1519895-G-A
gnomAD v4:
16-1519895-G-A
COSMIC:
COSM5581347
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1519895G>A , CM000678.2:g.1519895G>A | GRCh38 |
| NC_000016.9:g.1569896G>A , CM000678.1:g.1569896G>A | GRCh37 |
| NC_000016.8:g.1509897G>A | NCBI36 |
| NG_032783.1:g.97214C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000426508.7:c.4026C>T MANE Select | ENSP00000406012.2:p.Phe1342= | |
| ENST00000361339.9:c.1608C>T | ENSP00000354895.5:p.Phe536= | |
| ENST00000397417.6:c.*2464C>T | ENSP00000380562.2:n.*2464C>T | |
| ENST00000426508.6:c.4026C>T | ENSP00000406012.2:p.Phe1342= | |
| ENST00000565298.5:n.3850C>T | ||
| ENST00000568837.1:c.144C>T | ENSP00000458439.1:p.Phe48= | |
| NM_014714.3:c.4026C>T | NP_055529.2:p.Phe1342= | |
| XM_006720989.2:c.4026C>T | XP_006721052.1:p.Phe1342= | |
| XM_006720990.2:c.4026C>T | XP_006721053.1:p.Phe1342= | |
| XM_006720991.2:c.4026C>T | XP_006721054.1:p.Phe1342= | |
| XM_006720992.2:c.1659C>T | XP_006721055.1:p.Phe553= | |
| XM_011522766.1:c.3780C>T | XP_011521068.1:p.Phe1260= | |
| XM_011522767.1:c.3051C>T | XP_011521069.1:p.Phe1017= | |
| XM_006720990.3:c.4026C>T | XP_006721053.1:p.Phe1342= | |
| XM_006720991.3:c.4026C>T | XP_006721054.1:p.Phe1342= | |
| XM_006720992.3:c.1659C>T | XP_006721055.1:p.Phe553= | |
| XM_011522766.3:c.3780C>T | XP_011521068.1:p.Phe1260= | |
| XM_011522767.2:c.3051C>T | XP_011521069.1:p.Phe1017= | |
| XM_017023910.1:c.4026C>T | XP_016879399.1:p.Phe1342= | |
| XM_017023911.1:c.2211C>T | XP_016879400.1:p.Phe737= | |
| NM_014714.4:c.4026C>T MANE Select | NP_055529.2:p.Phe1342= |