Linked Data
ClinVar Variation Id:
135922
dbSNP Id:
rs587780718
gnomAD v2:
19-1219395-A-G
gnomAD v3:
19-1219396-A-G
gnomAD v4:
19-1219396-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1219396A>G , CM000681.2:g.1219396A>G | GRCh38 |
| NC_000019.9:g.1219395A>G , CM000681.1:g.1219395A>G | GRCh37 |
| NC_000019.8:g.1170395A>G | NCBI36 |
| NG_007460.2:g.34990A>G , LRG_319:g.34990A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.447A>G | ENSP00000490268.2:p.Pro149= | |
| ENST00000585748.3:c.75A>G | ENSP00000477641.2:p.Pro25= | |
| ENST00000585851.2:c.291-977A>G | ENSP00000467912.2:n.291-977A>G | |
| ENST00000326873.12:c.447A>G MANE Select | ENSP00000324856.6:p.Pro149= | |
| ENST00000652231.1:c.447A>G | ENSP00000498804.1:p.Pro149= | |
| ENST00000326873.11:c.447A>G | ENSP00000324856.6:p.Pro149= | |
| ENST00000585851.1:c.291-977A>G | ENSP00000467912.1:n.291-977A>G | |
| ENST00000586243.5:c.447A>G | ENSP00000467240.2:p.Pro149= | |
| ENST00000586358.5:n.270A>G | ||
| ENST00000589152.5:n.537A>G | ||
| NM_000455.4:c.447A>G , LRG_319t1:c.447A>G | NP_000446.1:p.Pro149= | |
| XM_005259617.1:c.447A>G | XP_005259674.1:p.Pro149= | |
| XM_005259618.3:c.447A>G | XP_005259675.1:p.Pro149= | |
| XM_011528209.1:c.225A>G | XP_011526511.1:p.Pro75= | |
| XR_936204.1:n.1072A>G | ||
| XM_005259617.3:c.447A>G | XP_005259674.1:p.Pro149= | |
| XM_011528209.2:c.225A>G | XP_011526511.1:p.Pro75= | |
| XR_001753738.2:n.1072A>G | ||
| XR_001753739.1:n.1072A>G | ||
| XR_001753740.2:n.1072A>G | ||
| NM_000455.5:c.447A>G MANE Select | NP_000446.1:p.Pro149= |