Linked Data
ClinVar Variation Id:
1653784
ClinVar RCV Id:
RCV002161373
dbSNP Id:
rs767344852
ExAC:
19:36556931 G / A
gnomAD v2:
19-36556931-G-A
gnomAD v3:
19-36066029-G-A
gnomAD v4:
19-36066029-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.36066029G>A , CM000681.2:g.36066029G>A | GRCh38 |
| NC_000019.9:g.36556931G>A , CM000681.1:g.36556931G>A | GRCh37 |
| NC_000019.8:g.41248771G>A | NCBI36 |
| NG_028101.1:g.16149G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270301.12:c.390+14G>A | ENSP00000270301.6:n.390+14G>A | |
| ENST00000401500.7:c.390+14G>A MANE Select | ENSP00000384792.1:n.390+14G>A | |
| ENST00000427823.3:c.474+14G>A | ENSP00000413475.4:n.474+14G>A | |
| ENST00000587391.6:c.390+14G>A | ENSP00000465525.1:n.390+14G>A | |
| ENST00000589953.2:n.468G>A | ||
| ENST00000644764.2:c.390+14G>A | ENSP00000494253.2:n.390+14G>A | |
| ENST00000679682.1:c.390+14G>A | ENSP00000506226.1:n.390+14G>A | |
| ENST00000679714.1:c.390+14G>A | ENSP00000506627.1:n.390+14G>A | |
| ENST00000679757.1:c.390+14G>A | ENSP00000505158.1:n.390+14G>A | |
| ENST00000679858.1:c.390+14G>A | ENSP00000505655.1:n.390+14G>A | |
| ENST00000680321.1:c.390+14G>A | ENSP00000505525.1:n.390+14G>A | |
| ENST00000680359.1:c.390+14G>A | ENSP00000506079.1:n.390+14G>A | |
| ENST00000680403.1:c.390+14G>A | ENSP00000505677.1:n.390+14G>A | |
| ENST00000680489.1:n.713+14G>A | ||
| ENST00000680564.1:c.390+14G>A | ENSP00000505582.1:n.390+14G>A | |
| ENST00000680590.1:c.390+14G>A | ENSP00000505350.1:n.390+14G>A | |
| ENST00000680806.1:c.390+14G>A | ENSP00000506418.1:n.390+14G>A | |
| ENST00000681542.1:c.390+14G>A | ENSP00000505251.1:n.390+14G>A | |
| ENST00000681625.1:c.390+14G>A | ENSP00000505555.1:n.390+14G>A | |
| ENST00000681809.1:c.390+14G>A | ENSP00000505740.1:n.390+14G>A | |
| ENST00000270301.11:c.390+14G>A | ENSP00000270301.6:n.390+14G>A | |
| ENST00000378860.8:n.481+14G>A | ||
| ENST00000401500.6:c.390+14G>A | ENSP00000384792.1:n.390+14G>A | |
| ENST00000427823.2:c.456+14G>A | ENSP00000413475.3:n.456+14G>A | |
| ENST00000587391.5:c.390+14G>A | ENSP00000465525.1:n.390+14G>A | |
| NM_001083961.1:c.390+14G>A | NP_001077430.1:n.390+14G>A | |
| NM_173636.4:c.390+14G>A | NP_775907.4:n.390+14G>A | |
| XM_005258809.2:c.390+14G>A | XP_005258866.1:n.390+14G>A | |
| XM_011526837.1:c.390+14G>A | XP_011525139.1:n.390+14G>A | |
| XM_011526838.1:c.390+14G>A | XP_011525140.1:n.390+14G>A | |
| XM_011526839.1:c.390+14G>A | XP_011525141.1:n.390+14G>A | |
| XM_017026665.1:c.390+14G>A | XP_016882154.1:n.390+14G>A | |
| XR_001753671.1:n.481+14G>A | ||
| XR_001753672.1:n.481+14G>A | ||
| NM_001083961.2:c.390+14G>A MANE Select | NP_001077430.1:n.390+14G>A | |
| NM_173636.5:c.390+14G>A | NP_775907.4:n.390+14G>A |