Linked Data
ClinVar Variation Id:
256391
ClinVar RCV Id:
RCV000248525
RCV000287336
RCV000283830
RCV000323697
RCV000378251
RCV000721204
RCV001079516
dbSNP Id:
rs368360689
ExAC:
19:39016094 G / A
gnomAD v2:
19-39016094-G-A
gnomAD v3:
19-38525454-G-A
gnomAD v4:
19-38525454-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38525454G>A , CM000681.2:g.38525454G>A | GRCh38 |
| NC_000019.9:g.39016094G>A , CM000681.1:g.39016094G>A | GRCh37 |
| NC_000019.8:g.43707934G>A | NCBI36 |
| NG_008866.1:g.96755G>A , LRG_766:g.96755G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000599547.6:c.10517G>A | ENSP00000471601.2:n.10517G>A | |
| ENST00000359596.8:c.10578G>A MANE Select | ENSP00000352608.2:p.Ala3526= | |
| ENST00000355481.8:c.10563G>A | ENSP00000347667.3:p.Ala3521= | |
| ENST00000359596.7:c.10578G>A | ENSP00000352608.2:p.Ala3526= | |
| ENST00000360985.7:c.10560G>A | ENSP00000354254.4:p.Ala3520= | |
| ENST00000594335.5:c.3965G>A | ||
| ENST00000599547.5:c.1385G>A | ||
| NM_000540.2:c.10578G>A , LRG_766t1:c.10578G>A | NP_000531.2:p.Ala3526= | |
| NM_001042723.1:c.10563G>A | NP_001036188.1:p.Ala3521= | |
| XM_006723317.1:c.10578G>A | XP_006723380.1:p.Ala3526= | |
| XM_006723319.1:c.10563G>A | XP_006723382.1:p.Ala3521= | |
| XM_011527204.1:c.10575G>A | XP_011525506.1:p.Ala3525= | |
| XM_011527205.1:c.10578G>A | XP_011525507.1:p.Ala3526= | |
| XM_006723317.2:c.10578G>A | XP_006723380.1:p.Ala3526= | |
| XM_006723319.2:c.10563G>A | XP_006723382.1:p.Ala3521= | |
| XM_011527205.2:c.10578G>A | XP_011525507.1:p.Ala3526= | |
| NM_000540.3:c.10578G>A MANE Select | NP_000531.2:p.Ala3526= | |
| NM_001042723.2:c.10563G>A | NP_001036188.1:p.Ala3521= |