Linked Data
ClinVar Variation Id:
321362
dbSNP Id:
rs773318145
ExAC:
16:89858351 C / T
gnomAD v2:
16-89858351-C-T
gnomAD v3:
16-89791943-C-T
gnomAD v4:
16-89791943-C-T
COSMIC:
COSM6224618
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89791943C>T , CM000678.2:g.89791943C>T | GRCh38 |
| NC_000016.9:g.89858351C>T , CM000678.1:g.89858351C>T | GRCh37 |
| NC_000016.8:g.88385852C>T | NCBI36 |
| NG_011706.1:g.29715G>A , LRG_495:g.29715G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561667.2:c.1209G>A | ENSP00000512522.1:p.Ala403= | |
| ENST00000563767.2:n.1104G>A | ||
| ENST00000564475.6:c.1209G>A | ENSP00000454977.2:p.Ala403= | |
| ENST00000567205.2:c.1209G>A | ENSP00000457027.2:p.Ala403= | |
| ENST00000567284.7:n.1252G>A | ||
| ENST00000567621.6:c.*196G>A | ENSP00000456762.2:n.*196G>A | |
| ENST00000568369.6:c.1209G>A | ENSP00000456829.1:p.Ala403= | |
| ENST00000696274.1:n.1170G>A | ||
| ENST00000696275.1:c.*444G>A | ENSP00000512517.1:n.*444G>A | |
| ENST00000696276.1:n.1252G>A | ||
| ENST00000696277.1:c.1209G>A | ENSP00000512518.1:p.Ala403= | |
| ENST00000696286.1:c.1209G>A | ENSP00000512523.1:p.Ala403= | |
| ENST00000696287.1:c.1209G>A | ENSP00000512524.1:p.Ala403= | |
| ENST00000696291.1:c.*553G>A | ENSP00000512530.1:n.*553G>A | |
| ENST00000696292.1:c.1289G>A | ENSP00000512531.1:n.1289G>A | |
| ENST00000389301.8:c.1209G>A MANE Select | ENSP00000373952.3:p.Ala403= | |
| ENST00000389301.7:c.1209G>A | ENSP00000373952.3:p.Ala403= | |
| ENST00000563767.1:n.69G>A | ||
| ENST00000566133.1:n.381G>A | ||
| ENST00000567621.5:c.573G>A | ||
| ENST00000568369.5:c.1209G>A | ENSP00000456829.1:p.Ala403= | |
| NM_000135.2:c.1209G>A , LRG_495t1:c.1209G>A | NP_000126.2:p.Ala403= | |
| NM_001286167.1:c.1209G>A | NP_001273096.1:p.Ala403= | |
| XM_005256294.3:c.1209G>A | XP_005256351.1:p.Ala403= | |
| XM_011522945.1:c.1209G>A | XP_011521247.1:p.Ala403= | |
| XM_011522946.1:c.186G>A | XP_011521248.1:p.Ala62= | |
| XM_011522947.1:c.186G>A | XP_011521249.1:p.Ala62= | |
| XM_011522948.1:c.1209G>A | XP_011521250.1:p.Ala403= | |
| XR_933244.1:n.1252G>A | ||
| XR_933245.1:n.1252G>A | ||
| XR_933246.1:n.1252G>A | ||
| XR_933247.1:n.1252G>A | ||
| NM_000135.3:c.1209G>A | NP_000126.2:p.Ala403= | |
| NM_001286167.2:c.1209G>A | NP_001273096.1:p.Ala403= | |
| XM_005256294.4:c.1209G>A | XP_005256351.1:p.Ala403= | |
| XM_011522945.2:c.1209G>A | XP_011521247.1:p.Ala403= | |
| XM_011522946.3:c.186G>A | XP_011521248.1:p.Ala62= | |
| XM_011522947.2:c.186G>A | XP_011521249.1:p.Ala62= | |
| XM_011522948.2:c.1209G>A | XP_011521250.1:p.Ala403= | |
| XM_017023044.2:c.1209G>A | XP_016878533.1:p.Ala403= | |
| XM_017023045.1:c.1209G>A | XP_016878534.1:p.Ala403= | |
| XM_017023046.1:c.1209G>A | XP_016878535.1:p.Ala403= | |
| XM_024450189.1:c.186G>A | XP_024305957.1:p.Ala62= | |
| XR_001751866.1:n.1252G>A | ||
| XR_001751867.1:n.1252G>A | ||
| XR_001751868.2:n.1139G>A | ||
| XR_002957793.1:n.1381G>A | ||
| XR_933244.2:n.1252G>A | ||
| XR_933245.2:n.1252G>A | ||
| XR_933247.2:n.1252G>A | ||
| NM_000135.4:c.1209G>A MANE Select | NP_000126.2:p.Ala403= | |
| NM_001286167.3:c.1209G>A | NP_001273096.1:p.Ala403= |