Linked Data
ClinVar Variation Id:
329519
dbSNP Id:
rs529824119
ExAC:
19:45867235 G / A
gnomAD v2:
19-45867235-G-A
gnomAD v3:
19-45363977-G-A
gnomAD v4:
19-45363977-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.45363977G>A , CM000681.2:g.45363977G>A | GRCh38 |
| NC_000019.9:g.45867235G>A , CM000681.1:g.45867235G>A | GRCh37 |
| NC_000019.8:g.50559075G>A | NCBI36 |
| NG_007067.2:g.11611C>T , LRG_461:g.11611C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000391944.8:c.949+9C>T | ENSP00000375808.4:n.949+9C>T | |
| ENST00000682414.1:c.949+9C>T | ENSP00000507019.1:n.949+9C>T | |
| ENST00000682508.1:n.978+9C>T | ||
| ENST00000684218.1:c.*207+9C>T | ENSP00000507804.1:n.*207+9C>T | |
| ENST00000684407.1:c.826+9C>T | ENSP00000507775.1:n.826+9C>T | |
| ENST00000684458.1:c.949+9C>T | ENSP00000508260.1:n.949+9C>T | |
| ENST00000391945.10:c.949+9C>T MANE Select | ENSP00000375809.4:n.949+9C>T | |
| ENST00000587376.6:c.72+9C>T | ||
| ENST00000646507.1:n.1046+9C>T | ||
| ENST00000391941.6:c.877+9C>T | ENSP00000375805.2:n.877+9C>T | |
| ENST00000391944.7:c.715+9C>T | ENSP00000375808.3:n.715+9C>T | |
| ENST00000391945.8:c.949+9C>T | ENSP00000375809.3:n.949+9C>T | |
| ENST00000485403.6:c.877+9C>T | ENSP00000431229.2:n.877+9C>T | |
| ENST00000587376.5:c.72+9C>T | ||
| NM_000400.3:c.949+9C>T , LRG_461t1:c.949+9C>T | NP_000391.1:n.949+9C>T | |
| NM_001130867.1:c.877+9C>T | NP_001124339.1:n.877+9C>T | |
| XM_011526611.1:c.871+9C>T | XP_011524913.1:n.871+9C>T | |
| XR_935763.1:n.996+9C>T | ||
| XM_011526611.2:c.871+9C>T | XP_011524913.1:n.871+9C>T | |
| XM_017026467.1:c.826+9C>T | XP_016881956.1:n.826+9C>T | |
| XR_001753633.2:n.996+9C>T | ||
| XR_001753634.2:n.996+9C>T | ||
| NM_000400.4:c.949+9C>T MANE Select | NP_000391.1:n.949+9C>T | |
| NM_001130867.2:c.877+9C>T | NP_001124339.1:n.877+9C>T |