Linked Data
ClinVar Variation Id:
478196
dbSNP Id:
rs200002533
ExAC:
19:39068843 A / G
gnomAD v2:
19-39068843-A-G
gnomAD v3:
19-38578203-A-G
gnomAD v4:
19-38578203-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38578203A>G , CM000681.2:g.38578203A>G | GRCh38 |
| NC_000019.9:g.39068843A>G , CM000681.1:g.39068843A>G | GRCh37 |
| NC_000019.8:g.43760683A>G | NCBI36 |
| NG_008866.1:g.149504A>G , LRG_766:g.149504A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000593677.2:c.1299A>G | ||
| ENST00000688602.1:c.2696A>G | ||
| ENST00000689936.1:c.2668A>G | ||
| ENST00000359596.8:c.14363A>G MANE Select | ENSP00000352608.2:p.Asn4788Ser | |
| ENST00000355481.8:c.14348A>G | ENSP00000347667.3:p.Asn4783Ser | |
| ENST00000359596.7:c.14363A>G | ENSP00000352608.2:p.Asn4788Ser | |
| ENST00000360985.7:c.14345A>G | ENSP00000354254.4:p.Asn4782Ser | |
| NM_000540.2:c.14363A>G , LRG_766t1:c.14363A>G | NP_000531.2:p.Asn4788Ser | |
| NM_001042723.1:c.14348A>G | NP_001036188.1:p.Asn4783Ser | |
| XM_006723317.1:c.14345A>G | XP_006723380.1:p.Asn4782Ser | |
| XM_006723319.1:c.14330A>G | XP_006723382.1:p.Asn4777Ser | |
| XM_011527204.1:c.14360A>G | XP_011525506.1:p.Asn4787Ser | |
| XM_011527205.1:c.14276A>G | XP_011525507.1:p.Asn4759Ser | |
| XM_006723317.2:c.14345A>G | XP_006723380.1:p.Asn4782Ser | |
| XM_006723319.2:c.14330A>G | XP_006723382.1:p.Asn4777Ser | |
| XM_011527205.2:c.14276A>G | XP_011525507.1:p.Asn4759Ser | |
| NM_000540.3:c.14363A>G MANE Select | NP_000531.2:p.Asn4788Ser | |
| NM_001042723.2:c.14348A>G | NP_001036188.1:p.Asn4783Ser |