Linked Data
ClinVar Variation Id:
643945
dbSNP Id:
rs1337566743
gnomAD v2:
19-39056085-G-A
gnomAD v3:
19-38565445-G-A
gnomAD v4:
19-38565445-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38565445G>A , CM000681.2:g.38565445G>A | GRCh38 |
| NC_000019.9:g.39056085G>A , CM000681.1:g.39056085G>A | GRCh37 |
| NC_000019.8:g.43747925G>A | NCBI36 |
| NG_008866.1:g.136746G>A , LRG_766:g.136746G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000593677.2:c.47G>A | ||
| ENST00000688602.1:c.1521G>A | ||
| ENST00000689936.1:c.1503G>A | ||
| ENST00000359596.8:c.13111G>A MANE Select | ENSP00000352608.2:p.Ala4371Thr | |
| ENST00000355481.8:c.13096G>A | ENSP00000347667.3:p.Ala4366Thr | |
| ENST00000359596.7:c.13111G>A | ENSP00000352608.2:p.Ala4371Thr | |
| ENST00000360985.7:c.13093G>A | ENSP00000354254.4:p.Ala4365Thr | |
| NM_000540.2:c.13111G>A , LRG_766t1:c.13111G>A | NP_000531.2:p.Ala4371Thr | |
| NM_001042723.1:c.13096G>A | NP_001036188.1:p.Ala4366Thr | |
| XM_006723317.1:c.13093G>A | XP_006723380.1:p.Ala4365Thr | |
| XM_006723319.1:c.13078G>A | XP_006723382.1:p.Ala4360Thr | |
| XM_011527204.1:c.13108G>A | XP_011525506.1:p.Ala4370Thr | |
| XM_011527205.1:c.13111G>A | XP_011525507.1:p.Ala4371Thr | |
| XM_006723317.2:c.13093G>A | XP_006723380.1:p.Ala4365Thr | |
| XM_006723319.2:c.13078G>A | XP_006723382.1:p.Ala4360Thr | |
| XM_011527205.2:c.13111G>A | XP_011525507.1:p.Ala4371Thr | |
| NM_000540.3:c.13111G>A MANE Select | NP_000531.2:p.Ala4371Thr | |
| NM_001042723.2:c.13096G>A | NP_001036188.1:p.Ala4366Thr |