Linked Data
ClinVar Variation Id:
657657
ClinVar RCV Id:
RCV000814312
dbSNP Id:
rs878853986
gnomAD v4:
19-1226598-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1226598G>A , CM000681.2:g.1226598G>A | GRCh38 |
| NC_000019.9:g.1226597G>A , CM000681.1:g.1226597G>A | GRCh37 |
| NC_000019.8:g.1177597G>A | NCBI36 |
| NG_007460.2:g.42192G>A , LRG_319:g.42192G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.*2854G>A | ENSP00000490268.2:n.*2854G>A | |
| ENST00000585748.3:c.881G>A | ENSP00000477641.2:p.Cys294Tyr | |
| ENST00000585851.2:c.1079G>A | ENSP00000467912.2:p.Cys360Tyr | |
| ENST00000326873.12:c.1253G>A MANE Select | ENSP00000324856.6:p.Cys418Tyr | |
| ENST00000326873.11:c.1253G>A | ENSP00000324856.6:p.Cys418Tyr | |
| ENST00000585465.2:n.2986G>A | ||
| ENST00000586243.5:c.1252G>A | ENSP00000467240.2:p.Ala418Thr | |
| ENST00000589152.5:n.1951G>A | ||
| NM_000455.4:c.1253G>A , LRG_319t1:c.1253G>A | NP_000446.1:p.Cys418Tyr | |
| XM_005259617.1:c.1248G>A | XP_005259674.1:p.Leu416= | |
| XM_011528209.1:c.1026G>A | XP_011526511.1:p.Leu342= | |
| XM_005259617.3:c.1248G>A | XP_005259674.1:p.Leu416= | |
| XM_011528209.2:c.1026G>A | XP_011526511.1:p.Leu342= | |
| XR_001753738.2:n.2059G>A | ||
| XR_001753740.2:n.2029G>A | ||
| NM_000455.5:c.1253G>A MANE Select | NP_000446.1:p.Cys418Tyr |