Linked Data
ClinVar Variation Id:
3004160
ClinVar RCV Id:
RCV003865799
dbSNP Id:
rs1446241725
gnomAD v2:
19-38976410-A-G
gnomAD v3:
19-38485770-A-G
gnomAD v4:
19-38485770-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38485770A>G , CM000681.2:g.38485770A>G | GRCh38 |
| NC_000019.9:g.38976410A>G , CM000681.1:g.38976410A>G | GRCh37 |
| NC_000019.8:g.43668250A>G | NCBI36 |
| NG_008866.1:g.57071A>G , LRG_766:g.57071A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000599547.6:c.5115A>G | ENSP00000471601.2:p.Pro1705= | |
| ENST00000359596.8:c.5115A>G MANE Select | ENSP00000352608.2:p.Pro1705= | |
| ENST00000355481.8:c.5115A>G | ENSP00000347667.3:p.Pro1705= | |
| ENST00000359596.7:c.5115A>G | ENSP00000352608.2:p.Pro1705= | |
| ENST00000360985.7:c.5112A>G | ENSP00000354254.4:p.Pro1704= | |
| NM_000540.2:c.5115A>G , LRG_766t1:c.5115A>G | NP_000531.2:p.Pro1705= | |
| NM_001042723.1:c.5115A>G | NP_001036188.1:p.Pro1705= | |
| XM_006723317.1:c.5115A>G | XP_006723380.1:p.Pro1705= | |
| XM_006723319.1:c.5115A>G | XP_006723382.1:p.Pro1705= | |
| XM_011527204.1:c.5112A>G | XP_011525506.1:p.Pro1704= | |
| XM_011527205.1:c.5115A>G | XP_011525507.1:p.Pro1705= | |
| XM_006723317.2:c.5115A>G | XP_006723380.1:p.Pro1705= | |
| XM_006723319.2:c.5115A>G | XP_006723382.1:p.Pro1705= | |
| XM_011527205.2:c.5115A>G | XP_011525507.1:p.Pro1705= | |
| XR_001753735.1:n.5198A>G | ||
| NM_000540.3:c.5115A>G MANE Select | NP_000531.2:p.Pro1705= | |
| NM_001042723.2:c.5115A>G | NP_001036188.1:p.Pro1705= |